Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 9096 |
| ensemblid | ENSG00000112837.17 |
| hgncid | 11595 |
| symbol | TBX18 |
| name | T-box transcription factor 18 |
| refseq_nuc | NM_001080508.3 |
| refseq_prot | NP_001073977.1 |
| ensembl_nuc | ENST00000369663.10 |
| ensembl_prot | ENSP00000358677.4 |
| mane_status | MANE Select |
| chr | chr6 |
| start | 84732496 |
| end | 84764598 |
| strand | - |
| ver | v1.2 |
| region | chr6:84732496-84764598 |
| region5000 | chr6:84727496-84769598 |
| regionname0 | TBX18_chr6_84732496_84764598 |
| regionname5000 | TBX18_chr6_84727496_84769598 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/0 | 607 | 247 | 84 | 48 | 91 | 11 | 12 | 74 | TBX18_chr6_84727496_84769598 | TBX18 | MAEKR others(602): Show |
chr6 | 84727496 | 84769598 |
| a0002 | 0/1 | 607 | 146 | 6 | 25 | 83 | 5 | 26 | 62 | TBX18_chr6_84727496_84769598 | TBX18 | MAEKR others(602): Show |
chr6 | 84727496 | 84769598 |
| a0003 | 0/0 | 607 | 3 | 0 | 0 | 0 | 0 | 3 | 0 | TBX18_chr6_84727496_84769598 | TBX18 | MAEKR others(602): Show |
chr6 | 84727496 | 84769598 |
| a0004 | 0/0 | 607 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | TBX18_chr6_84727496_84769598 | TBX18 | MAEKR others(602): Show |
chr6 | 84727496 | 84769598 |
| a0005 | 0/0 | 611 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | TBX18_chr6_84727496_84769598 | TBX18 | MAEKR others(606): Show |
chr6 | 84727496 | 84769598 |
| a0006 | 0/0 | 607 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | TBX18_chr6_84727496_84769598 | TBX18 | MAEKR others(602): Show |
chr6 | 84727496 | 84769598 |
| a0007 | 0/0 | 607 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | TBX18_chr6_84727496_84769598 | TBX18 | MAEKR others(602): Show |
chr6 | 84727496 | 84769598 |
| a0008 | 0/0 | 607 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TBX18_chr6_84727496_84769598 | TBX18 | MAEKR others(602): Show |
chr6 | 84727496 | 84769598 |
| a0009 | 0/0 | 607 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TBX18_chr6_84727496_84769598 | TBX18 | MAEKR others(602): Show |
chr6 | 84727496 | 84769598 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/0 | 1821 | 240 | 82 | 48 | 86 | 11 | 12 | TBX18_chr6_84727496_84769598 | TBX18 | ATGGC others(1816): Show |
chr6 | 84727496 | 84769598 | ||
| a0001c0003 | 0/0 | 1821 | 3 | 0 | 0 | 3 | 0 | 0 | TBX18_chr6_84727496_84769598 | TBX18 | ATGGC others(1816): Show |
chr6 | 84727496 | 84769598 | ||
| a0001c0007 | 0/0 | 1821 | 2 | 0 | 0 | 2 | 0 | 0 | TBX18_chr6_84727496_84769598 | TBX18 | ATGGC others(1816): Show |
chr6 | 84727496 | 84769598 | ||
| a0001c0014 | 0/0 | 1821 | 1 | 1 | 0 | 0 | 0 | 0 | TBX18_chr6_84727496_84769598 | TBX18 | ATGGC others(1816): Show |
chr6 | 84727496 | 84769598 | ||
| a0001c0015 | 0/0 | 1821 | 1 | 1 | 0 | 0 | 0 | 0 | TBX18_chr6_84727496_84769598 | TBX18 | ATGGC others(1816): Show |
chr6 | 84727496 | 84769598 | ||
| a0002c0002 | 0/1 | 1821 | 144 | 6 | 25 | 81 | 5 | 26 | TBX18_chr6_84727496_84769598 | TBX18 | ATGGC others(1816): Show |
chr6 | 84727496 | 84769598 | ||
| a0002c0008 | 0/0 | 1821 | 1 | 0 | 0 | 1 | 0 | 0 | TBX18_chr6_84727496_84769598 | TBX18 | ATGGC others(1816): Show |
chr6 | 84727496 | 84769598 | ||
| a0002c0009 | 0/0 | 1821 | 1 | 0 | 0 | 1 | 0 | 0 | TBX18_chr6_84727496_84769598 | TBX18 | ATGGC others(1816): Show |
chr6 | 84727496 | 84769598 | ||
| a0003c0004 | 0/0 | 1821 | 3 | 0 | 0 | 0 | 0 | 3 | TBX18_chr6_84727496_84769598 | TBX18 | ATGGC others(1816): Show |
chr6 | 84727496 | 84769598 | ||
| a0004c0006 | 0/0 | 1821 | 2 | 2 | 0 | 0 | 0 | 0 | TBX18_chr6_84727496_84769598 | TBX18 | ATGGC others(1816): Show |
chr6 | 84727496 | 84769598 | ||
| a0005c0005 | 0/0 | 1833 | 2 | 0 | 0 | 2 | 0 | 0 | TBX18_chr6_84727496_84769598 | TBX18 | ATGGC others(1828): Show |
chr6 | 84727496 | 84769598 | ||
| a0006c0013 | 0/0 | 1821 | 1 | 0 | 1 | 0 | 0 | 0 | TBX18_chr6_84727496_84769598 | TBX18 | ATGGC others(1816): Show |
chr6 | 84727496 | 84769598 | ||
| a0007c0012 | 0/0 | 1821 | 1 | 0 | 0 | 0 | 0 | 1 | TBX18_chr6_84727496_84769598 | TBX18 | ATGGC others(1816): Show |
chr6 | 84727496 | 84769598 | ||
| a0008c0011 | 0/0 | 1821 | 1 | 1 | 0 | 0 | 0 | 0 | TBX18_chr6_84727496_84769598 | TBX18 | ATGGC others(1816): Show |
chr6 | 84727496 | 84769598 | ||
| a0009c0010 | 0/0 | 1821 | 1 | 1 | 0 | 0 | 0 | 0 | TBX18_chr6_84727496_84769598 | TBX18 | ATGGC others(1816): Show |
chr6 | 84727496 | 84769598 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 6430 | 2 | 0 | 2 | 0 | 0 | 0 | TBX18_chr6_84727496_84769598 | TBX18 | ACCGC others(6425): Show |
chr6 | 84727496 | 84769598 |
| a0001c0001t0002 | 0/0 | 6430 | 75 | 0 | 21 | 49 | 2 | 3 | TBX18_chr6_84727496_84769598 | TBX18 | ACCGC others(6425): Show |
chr6 | 84727496 | 84769598 |
| a0001c0001t0003 | 0/0 | 6428 | 14 | 5 | 2 | 0 | 1 | 6 | TBX18_chr6_84727496_84769598 | TBX18 | ACCGC others(6423): Show |
chr6 | 84727496 | 84769598 |
| a0001c0001t0004 | 1/0 | 6430 | 50 | 5 | 12 | 25 | 5 | 2 | TBX18_chr6_84727496_84769598 | TBX18 | ACCGC others(6425): Show |
chr6 | 84727496 | 84769598 |
| a0001c0001t0005 | 0/0 | 6432 | 20 | 7 | 5 | 5 | 2 | 1 | TBX18_chr6_84727496_84769598 | TBX18 | ACCGC others(6427): Show |
chr6 | 84727496 | 84769598 |
| a0001c0001t0006 | 0/0 | 6430 | 10 | 6 | 3 | 0 | 1 | 0 | TBX18_chr6_84727496_84769598 | TBX18 | ACCGC others(6425): Show |
chr6 | 84727496 | 84769598 |
| a0001c0001t0007 | 0/0 | 6432 | 12 | 11 | 1 | 0 | 0 | 0 | TBX18_chr6_84727496_84769598 | TBX18 | ACCGC others(6427): Show |
chr6 | 84727496 | 84769598 |
| a0001c0001t0008 | 0/0 | 6432 | 11 | 11 | 0 | 0 | 0 | 0 | TBX18_chr6_84727496_84769598 | TBX18 | ACCGC others(6427): Show |
chr6 | 84727496 | 84769598 |
| a0001c0001t0009 | 0/0 | 6432 | 10 | 10 | 0 | 0 | 0 | 0 | TBX18_chr6_84727496_84769598 | TBX18 | ACCGC others(6427): Show |
chr6 | 84727496 | 84769598 |
| a0001c0001t0010 | 0/0 | 6432 | 6 | 6 | 0 | 0 | 0 | 0 | TBX18_chr6_84727496_84769598 | TBX18 | ACCGC others(6427): Show |
chr6 | 84727496 | 84769598 |
| a0001c0001t0011 | 0/0 | 6430 | 6 | 5 | 1 | 0 | 0 | 0 | TBX18_chr6_84727496_84769598 | TBX18 | ACCGC others(6425): Show |
chr6 | 84727496 | 84769598 |
| a0001c0001t0012 | 0/0 | 6428 | 5 | 5 | 0 | 0 | 0 | 0 | TBX18_chr6_84727496_84769598 | TBX18 | ACCGC others(6423): Show |
chr6 | 84727496 | 84769598 |
| a0001c0001t0013 | 0/0 | 6432 | 3 | 3 | 0 | 0 | 0 | 0 | TBX18_chr6_84727496_84769598 | TBX18 | ACCGC others(6427): Show |
chr6 | 84727496 | 84769598 |
| a0001c0001t0015 | 0/0 | 6430 | 2 | 0 | 0 | 2 | 0 | 0 | TBX18_chr6_84727496_84769598 | TBX18 | ACCGC others(6425): Show |
chr6 | 84727496 | 84769598 |
| a0001c0001t0016 | 0/0 | 6428 | 2 | 1 | 1 | 0 | 0 | 0 | TBX18_chr6_84727496_84769598 | TBX18 | ACCGC others(6423): Show |
chr6 | 84727496 | 84769598 |
| a0001c0001t0017 | 0/0 | 6430 | 2 | 0 | 0 | 2 | 0 | 0 | TBX18_chr6_84727496_84769598 | TBX18 | ACCGC others(6425): Show |
chr6 | 84727496 | 84769598 |
| a0001c0001t0018 | 0/0 | 6430 | 1 | 1 | 0 | 0 | 0 | 0 | TBX18_chr6_84727496_84769598 | TBX18 | ACCGC others(6425): Show |
chr6 | 84727496 | 84769598 |
| a0001c0001t0020 | 0/0 | 6432 | 1 | 1 | 0 | 0 | 0 | 0 | TBX18_chr6_84727496_84769598 | TBX18 | ACCGC others(6427): Show |
chr6 | 84727496 | 84769598 |
| a0001c0001t0021 | 0/0 | 6432 | 1 | 1 | 0 | 0 | 0 | 0 | TBX18_chr6_84727496_84769598 | TBX18 | ACCGC others(6427): Show |
chr6 | 84727496 | 84769598 |
| a0001c0001t0022 | 0/0 | 6432 | 1 | 1 | 0 | 0 | 0 | 0 | TBX18_chr6_84727496_84769598 | TBX18 | ACCGC others(6427): Show |
chr6 | 84727496 | 84769598 |
| a0001c0001t0025 | 0/0 | 6430 | 1 | 0 | 0 | 1 | 0 | 0 | TBX18_chr6_84727496_84769598 | TBX18 | ACCGC others(6425): Show |
chr6 | 84727496 | 84769598 |
| a0001c0001t0027 | 0/0 | 6430 | 1 | 0 | 0 | 1 | 0 | 0 | TBX18_chr6_84727496_84769598 | TBX18 | ACCGC others(6425): Show |
chr6 | 84727496 | 84769598 |
| a0001c0001t0028 | 0/0 | 6430 | 1 | 0 | 0 | 1 | 0 | 0 | TBX18_chr6_84727496_84769598 | TBX18 | ACCGC others(6425): Show |
chr6 | 84727496 | 84769598 |
| a0001c0001t0029 | 0/0 | 6430 | 1 | 1 | 0 | 0 | 0 | 0 | TBX18_chr6_84727496_84769598 | TBX18 | ACCGC others(6425): Show |
chr6 | 84727496 | 84769598 |
| a0001c0001t0030 | 0/0 | 6430 | 1 | 1 | 0 | 0 | 0 | 0 | TBX18_chr6_84727496_84769598 | TBX18 | ACCGC others(6425): Show |
chr6 | 84727496 | 84769598 |
| a0001c0001t0033 | 0/0 | 6430 | 1 | 1 | 0 | 0 | 0 | 0 | TBX18_chr6_84727496_84769598 | TBX18 | ACCGC others(6425): Show |
chr6 | 84727496 | 84769598 |
| a0001c0003t0004 | 0/0 | 6430 | 3 | 0 | 0 | 3 | 0 | 0 | TBX18_chr6_84727496_84769598 | TBX18 | ACCGC others(6425): Show |
chr6 | 84727496 | 84769598 |
| a0001c0007t0001 | 0/0 | 6430 | 1 | 0 | 0 | 1 | 0 | 0 | TBX18_chr6_84727496_84769598 | TBX18 | ACCGC others(6425): Show |
chr6 | 84727496 | 84769598 |
| a0001c0007t0034 | 0/0 | 6430 | 1 | 0 | 0 | 1 | 0 | 0 | TBX18_chr6_84727496_84769598 | TBX18 | ACCGC others(6425): Show |
chr6 | 84727496 | 84769598 |
| a0001c0014t0006 | 0/0 | 6430 | 1 | 1 | 0 | 0 | 0 | 0 | TBX18_chr6_84727496_84769598 | TBX18 | ACCGC others(6425): Show |
chr6 | 84727496 | 84769598 |
| a0001c0015t0003 | 0/0 | 6428 | 1 | 1 | 0 | 0 | 0 | 0 | TBX18_chr6_84727496_84769598 | TBX18 | ACCGC others(6423): Show |
chr6 | 84727496 | 84769598 |
| a0002c0002t0001 | 0/0 | 6430 | 87 | 1 | 13 | 59 | 1 | 13 | TBX18_chr6_84727496_84769598 | TBX18 | ACCGC others(6425): Show |
chr6 | 84727496 | 84769598 |
| a0002c0002t0003 | 0/1 | 6428 | 47 | 3 | 12 | 17 | 4 | 10 | TBX18_chr6_84727496_84769598 | TBX18 | ACCGC others(6423): Show |
chr6 | 84727496 | 84769598 |
| a0002c0002t0005 | 0/0 | 6432 | 1 | 0 | 0 | 0 | 0 | 1 | TBX18_chr6_84727496_84769598 | TBX18 | ACCGC others(6427): Show |
chr6 | 84727496 | 84769598 |
| a0002c0002t0012 | 0/0 | 6428 | 1 | 1 | 0 | 0 | 0 | 0 | TBX18_chr6_84727496_84769598 | TBX18 | ACCGC others(6423): Show |
chr6 | 84727496 | 84769598 |
| a0002c0002t0019 | 0/0 | 6430 | 1 | 0 | 0 | 1 | 0 | 0 | TBX18_chr6_84727496_84769598 | TBX18 | ACCGC others(6425): Show |
chr6 | 84727496 | 84769598 |
| a0002c0002t0023 | 0/0 | 6428 | 1 | 0 | 0 | 1 | 0 | 0 | TBX18_chr6_84727496_84769598 | TBX18 | ACCGC others(6423): Show |
chr6 | 84727496 | 84769598 |
| a0002c0002t0024 | 0/0 | 6430 | 1 | 0 | 0 | 1 | 0 | 0 | TBX18_chr6_84727496_84769598 | TBX18 | ACCGC others(6425): Show |
chr6 | 84727496 | 84769598 |
| a0002c0002t0026 | 0/0 | 6430 | 1 | 0 | 0 | 0 | 0 | 1 | TBX18_chr6_84727496_84769598 | TBX18 | ACCGC others(6425): Show |
chr6 | 84727496 | 84769598 |
| a0002c0002t0031 | 0/0 | 6430 | 1 | 0 | 0 | 1 | 0 | 0 | TBX18_chr6_84727496_84769598 | TBX18 | ACCGC others(6425): Show |
chr6 | 84727496 | 84769598 |
| a0002c0002t0035 | 0/0 | 6430 | 1 | 0 | 0 | 0 | 0 | 1 | TBX18_chr6_84727496_84769598 | TBX18 | ACCGC others(6425): Show |
chr6 | 84727496 | 84769598 |
| a0002c0002t0037 | 0/0 | 6428 | 1 | 0 | 0 | 1 | 0 | 0 | TBX18_chr6_84727496_84769598 | TBX18 | ACCGC others(6423): Show |
chr6 | 84727496 | 84769598 |
| a0002c0002t0038 | 0/0 | 6430 | 1 | 1 | 0 | 0 | 0 | 0 | TBX18_chr6_84727496_84769598 | TBX18 | ACCGC others(6425): Show |
chr6 | 84727496 | 84769598 |
| a0002c0008t0001 | 0/0 | 6430 | 1 | 0 | 0 | 1 | 0 | 0 | TBX18_chr6_84727496_84769598 | TBX18 | ACCGC others(6425): Show |
chr6 | 84727496 | 84769598 |
| a0002c0009t0001 | 0/0 | 6430 | 1 | 0 | 0 | 1 | 0 | 0 | TBX18_chr6_84727496_84769598 | TBX18 | ACCGC others(6425): Show |
chr6 | 84727496 | 84769598 |
| a0003c0004t0001 | 0/0 | 6430 | 1 | 0 | 0 | 0 | 0 | 1 | TBX18_chr6_84727496_84769598 | TBX18 | ACCGC others(6425): Show |
chr6 | 84727496 | 84769598 |
| a0003c0004t0014 | 0/0 | 6430 | 2 | 0 | 0 | 0 | 0 | 2 | TBX18_chr6_84727496_84769598 | TBX18 | ACCGC others(6425): Show |
chr6 | 84727496 | 84769598 |
| a0004c0006t0006 | 0/0 | 6430 | 2 | 2 | 0 | 0 | 0 | 0 | TBX18_chr6_84727496_84769598 | TBX18 | ACCGC others(6425): Show |
chr6 | 84727496 | 84769598 |
| a0005c0005t0004 | 0/0 | 6442 | 1 | 0 | 0 | 1 | 0 | 0 | TBX18_chr6_84727496_84769598 | TBX18 | ACCGC others(6437): Show |
chr6 | 84727496 | 84769598 |
| a0005c0005t0032 | 0/0 | 6442 | 1 | 0 | 0 | 1 | 0 | 0 | TBX18_chr6_84727496_84769598 | TBX18 | ACCGC others(6437): Show |
chr6 | 84727496 | 84769598 |
| a0006c0013t0036 | 0/0 | 6428 | 1 | 0 | 1 | 0 | 0 | 0 | TBX18_chr6_84727496_84769598 | TBX18 | ACCGC others(6423): Show |
chr6 | 84727496 | 84769598 |
| a0007c0012t0003 | 0/0 | 6428 | 1 | 0 | 0 | 0 | 0 | 1 | TBX18_chr6_84727496_84769598 | TBX18 | ACCGC others(6423): Show |
chr6 | 84727496 | 84769598 |
| a0008c0011t0004 | 0/0 | 6430 | 1 | 1 | 0 | 0 | 0 | 0 | TBX18_chr6_84727496_84769598 | TBX18 | ACCGC others(6425): Show |
chr6 | 84727496 | 84769598 |
| a0009c0010t0006 | 0/0 | 6430 | 1 | 1 | 0 | 0 | 0 | 0 | TBX18_chr6_84727496_84769598 | TBX18 | ACCGC others(6425): Show |
chr6 | 84727496 | 84769598 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0035 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| a0001c0001t0002g0002 | 0/0 | 34 | 0 | 15 | 19 | 0 | 0 | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| a0001c0001t0002g0008 | 0/0 | 8 | 0 | 0 | 8 | 0 | 0 | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| a0001c0001t0002g0013 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| a0001c0001t0002g0016 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| a0001c0001t0002g0024 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| a0001c0001t0002g0041 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| a0001c0001t0002g0042 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| a0001c0001t0002g0043 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| a0001c0001t0002g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| a0001c0001t0002g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| a0001c0001t0002g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| a0001c0001t0002g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| a0001c0001t0002g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| a0001c0001t0002g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| a0001c0001t0002g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| a0001c0001t0002g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| a0001c0001t0002g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| a0001c0001t0002g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| a0001c0001t0002g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| a0001c0001t0002g0150 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| a0001c0001t0002g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| a0001c0001t0002g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| a0001c0001t0002g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| a0001c0001t0003g0005 | 0/0 | 10 | 1 | 2 | 0 | 1 | 6 | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| a0001c0001t0003g0039 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| a0001c0001t0003g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| a0001c0001t0003g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| a0001c0001t0004g0003 | 0/0 | 32 | 3 | 8 | 17 | 3 | 1 | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| a0001c0001t0004g0012 | 0/0 | 5 | 0 | 3 | 0 | 2 | 0 | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| a0001c0001t0004g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| a0001c0001t0004g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| a0001c0001t0004g0038 | 1/0 | 2 | 0 | 0 | 0 | 0 | 1 | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| a0001c0001t0004g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| a0001c0001t0004g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| a0001c0001t0004g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| a0001c0001t0004g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| a0001c0001t0004g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| a0001c0001t0004g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| a0001c0001t0004g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| a0001c0001t0005g0006 | 0/0 | 9 | 1 | 3 | 2 | 2 | 1 | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| a0001c0001t0005g0011 | 0/0 | 6 | 6 | 0 | 0 | 0 | 0 | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| a0001c0001t0005g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| a0001c0001t0005g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| a0001c0001t0005g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| a0001c0001t0005g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| a0001c0001t0006g0022 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| a0001c0001t0006g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| a0001c0001t0006g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| a0001c0001t0006g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| a0001c0001t0006g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| a0001c0001t0006g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| a0001c0001t0007g0014 | 0/0 | 5 | 4 | 1 | 0 | 0 | 0 | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| a0001c0001t0007g0018 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| a0001c0001t0007g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| a0001c0001t0007g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| a0001c0001t0007g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| a0001c0001t0008g0007 | 0/0 | 8 | 8 | 0 | 0 | 0 | 0 | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| a0001c0001t0008g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| a0001c0001t0008g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| a0001c0001t0008g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| a0001c0001t0009g0021 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| a0001c0001t0009g0023 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| a0001c0001t0009g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| a0001c0001t0009g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| a0001c0001t0009g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| a0001c0001t0009g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| a0001c0001t0010g0010 | 0/0 | 6 | 6 | 0 | 0 | 0 | 0 | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| a0001c0001t0011g0017 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| a0001c0001t0011g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| a0001c0001t0011g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| a0001c0001t0012g0044 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| a0001c0001t0012g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| a0001c0001t0012g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| a0001c0001t0012g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| a0001c0001t0013g0037 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| a0001c0001t0013g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| a0001c0001t0015g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| a0001c0001t0016g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| a0001c0001t0016g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| a0001c0001t0017g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| a0001c0001t0018g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| a0001c0001t0020g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| a0001c0001t0021g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| a0001c0001t0022g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| a0001c0001t0025g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| a0001c0001t0027g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| a0001c0001t0028g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| a0001c0001t0029g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| a0001c0001t0030g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| a0001c0001t0033g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| a0001c0003t0004g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| a0001c0003t0004g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| a0001c0007t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| a0001c0007t0034g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| a0001c0014t0006g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| a0001c0015t0003g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| a0002c0002t0001g0001 | 0/0 | 45 | 0 | 6 | 37 | 0 | 2 | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| a0002c0002t0001g0009 | 0/0 | 7 | 1 | 1 | 2 | 1 | 2 | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| a0002c0002t0001g0015 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| a0002c0002t0001g0019 | 0/0 | 3 | 0 | 1 | 1 | 0 | 1 | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| a0002c0002t0001g0020 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| a0002c0002t0001g0027 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| a0002c0002t0001g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| a0002c0002t0001g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| a0002c0002t0001g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| a0002c0002t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| a0002c0002t0001g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| a0002c0002t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| a0002c0002t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| a0002c0002t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| a0002c0002t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| a0002c0002t0001g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| a0002c0002t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| a0002c0002t0001g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| a0002c0002t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| a0002c0002t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| a0002c0002t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| a0002c0002t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| a0002c0002t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| a0002c0002t0001g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| a0002c0002t0001g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| a0002c0002t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| a0002c0002t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| a0002c0002t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| a0002c0002t0003g0004 | 0/1 | 30 | 0 | 8 | 12 | 2 | 7 | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| a0002c0002t0003g0028 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| a0002c0002t0003g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| a0002c0002t0003g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| a0002c0002t0003g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| a0002c0002t0003g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| a0002c0002t0003g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| a0002c0002t0003g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| a0002c0002t0003g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| a0002c0002t0003g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| a0002c0002t0003g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| a0002c0002t0003g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| a0002c0002t0003g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| a0002c0002t0003g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| a0002c0002t0003g0068 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| a0002c0002t0003g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| a0002c0002t0003g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| a0002c0002t0005g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| a0002c0002t0012g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| a0002c0002t0019g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| a0002c0002t0023g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| a0002c0002t0024g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| a0002c0002t0026g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| a0002c0002t0031g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| a0002c0002t0035g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| a0002c0002t0037g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| a0002c0002t0038g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| a0002c0008t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| a0002c0009t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| a0003c0004t0001g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| a0003c0004t0014g0025 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| a0004c0006t0006g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| a0004c0006t0006g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| a0005c0005t0004g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| a0005c0005t0032g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| a0006c0013t0036g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| a0007c0012t0003g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| a0008c0011t0004g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| a0009c0010t0006g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0002 | g0150 | EUR | GBR | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| HG00099 | hp2 | a0001 | c0001 | t0005 | g0006 | EUR | GBR | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| HG00140 | hp1 | a0001 | c0001 | t0002 | g0042 | EUR | GBR | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| HG00140 | hp2 | a0002 | c0002 | t0003 | g0028 | EUR | GBR | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| HG00280 | hp1 | a0002 | c0002 | t0003 | g0004 | EUR | FIN | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| HG00280 | hp2 | a0002 | c0002 | t0003 | g0068 | EUR | FIN | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| HG00408 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | CHS | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| HG00408 | hp2 | a0001 | c0001 | t0002 | g0163 | EAS | CHS | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| HG00423 | hp1 | a0001 | c0001 | t0025 | g0128 | EAS | CHS | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| HG00423 | hp2 | a0002 | c0002 | t0003 | g0004 | EAS | CHS | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| HG00438 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | CHS | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| HG00438 | hp2 | a0001 | c0001 | t0002 | g0043 | EAS | CHS | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| HG00544 | hp1 | a0002 | c0002 | t0001 | g0080 | EAS | CHS | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| HG00544 | hp2 | a0001 | c0001 | t0004 | g0125 | EAS | CHS | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| HG00597 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | CHS | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| HG00597 | hp2 | a0002 | c0002 | t0031 | g0086 | EAS | CHS | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| HG00609 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | CHS | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| HG00609 | hp2 | a0002 | c0002 | t0001 | g0015 | EAS | CHS | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| HG00639 | hp1 | a0002 | c0002 | t0001 | g0001 | AMR | PUR | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| HG00639 | hp2 | a0001 | c0001 | t0005 | g0136 | AMR | PUR | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| HG00642 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| HG00642 | hp2 | a0006 | c0013 | t0036 | g0126 | AMR | PUR | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| HG00673 | hp1 | a0001 | c0001 | t0004 | g0003 | EAS | CHS | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| HG00673 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | CHS | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| HG00733 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| HG00733 | hp2 | a0001 | c0001 | t0004 | g0003 | AMR | PUR | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| HG00735 | hp1 | a0002 | c0002 | t0001 | g0020 | AMR | PUR | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| HG00735 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0035 | AMR | PUR | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| HG00738 | hp2 | a0001 | c0001 | t0004 | g0003 | AMR | PUR | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| HG00741 | hp1 | a0001 | c0001 | t0004 | g0003 | AMR | PUR | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| HG00741 | hp2 | a0001 | c0001 | t0007 | g0014 | AMR | PUR | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| HG01069 | hp1 | a0002 | c0002 | t0003 | g0004 | AMR | PUR | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| HG01069 | hp2 | a0002 | c0002 | t0001 | g0001 | AMR | PUR | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| HG01070 | hp1 | a0002 | c0002 | t0003 | g0004 | AMR | PUR | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| HG01070 | hp2 | a0001 | c0001 | t0005 | g0137 | AMR | PUR | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| HG01071 | hp1 | a0002 | c0002 | t0001 | g0001 | AMR | PUR | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| HG01071 | hp2 | a0002 | c0002 | t0003 | g0004 | AMR | PUR | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| HG01074 | hp1 | a0001 | c0001 | t0004 | g0003 | AMR | PUR | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| HG01074 | hp2 | a0002 | c0002 | t0003 | g0028 | AMR | PUR | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| HG01081 | hp1 | a0002 | c0002 | t0003 | g0067 | AMR | PUR | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| HG01081 | hp2 | a0002 | c0002 | t0001 | g0019 | AMR | PUR | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| HG01099 | hp1 | a0002 | c0002 | t0003 | g0004 | AMR | PUR | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| HG01099 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| HG01106 | hp1 | a0001 | c0001 | t0006 | g0022 | AMR | PUR | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| HG01106 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| HG01109 | hp1 | a0001 | c0001 | t0016 | g0107 | AMR | PUR | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| HG01109 | hp2 | a0001 | c0001 | t0011 | g0017 | AMR | PUR | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| HG01167 | hp1 | a0001 | c0001 | t0002 | g0042 | AMR | PUR | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| HG01167 | hp2 | a0002 | c0002 | t0001 | g0073 | AMR | PUR | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| HG01168 | hp1 | a0002 | c0002 | t0003 | g0004 | AMR | PUR | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| HG01168 | hp2 | a0001 | c0001 | t0003 | g0005 | AMR | PUR | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| HG01169 | hp1 | a0002 | c0002 | t0003 | g0004 | AMR | PUR | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| HG01169 | hp2 | a0002 | c0002 | t0001 | g0072 | AMR | PUR | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| HG01175 | hp1 | a0001 | c0001 | t0004 | g0012 | AMR | PUR | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| HG01175 | hp2 | a0001 | c0001 | t0002 | g0041 | AMR | PUR | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| HG01192 | hp1 | a0001 | c0001 | t0004 | g0012 | AMR | PUR | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| HG01192 | hp2 | a0001 | c0001 | t0004 | g0003 | AMR | PUR | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| HG01243 | hp1 | a0001 | c0001 | t0004 | g0012 | AMR | PUR | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| HG01243 | hp2 | a0001 | c0001 | t0006 | g0131 | AMR | PUR | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| HG01255 | hp1 | a0002 | c0002 | t0001 | g0020 | AMR | CLM | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| HG01255 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | CLM | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| HG01256 | hp1 | a0001 | c0001 | t0005 | g0006 | AMR | CLM | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| HG01256 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | CLM | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| HG01257 | hp1 | a0001 | c0001 | t0002 | g0143 | AMR | CLM | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| HG01257 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | CLM | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| HG01261 | hp1 | a0001 | c0001 | t0002 | g0024 | AMR | CLM | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| HG01261 | hp2 | a0001 | c0001 | t0005 | g0006 | AMR | CLM | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| HG01346 | hp1 | a0001 | c0001 | t0005 | g0006 | AMR | CLM | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| HG01346 | hp2 | a0002 | c0002 | t0001 | g0001 | AMR | CLM | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| HG01433 | hp1 | a0001 | c0001 | t0004 | g0003 | AMR | CLM | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| HG01433 | hp2 | a0002 | c0002 | t0003 | g0060 | AMR | CLM | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| HG01496 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | CLM | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| HG01496 | hp2 | a0002 | c0002 | t0001 | g0001 | AMR | CLM | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| HG01515 | hp1 | a0001 | c0001 | t0005 | g0006 | EUR | IBS | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| HG01515 | hp2 | a0001 | c0001 | t0004 | g0003 | EUR | IBS | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| HG01516 | hp1 | a0001 | c0001 | t0006 | g0022 | EUR | IBS | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| HG01516 | hp2 | a0001 | c0001 | t0004 | g0012 | EUR | IBS | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| HG01517 | hp1 | a0001 | c0001 | t0004 | g0003 | EUR | IBS | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| HG01517 | hp2 | a0001 | c0001 | t0004 | g0012 | EUR | IBS | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| HG01884 | hp1 | a0001 | c0001 | t0012 | g0103 | AFR | ACB | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| HG01884 | hp2 | a0001 | c0001 | t0009 | g0129 | AFR | ACB | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| HG01891 | hp1 | a0001 | c0001 | t0008 | g0098 | AFR | ACB | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| HG01891 | hp2 | a0001 | c0001 | t0008 | g0007 | AFR | ACB | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| HG01934 | hp1 | a0001 | c0001 | t0006 | g0022 | AMR | PEL | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| HG01934 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | PEL | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| HG01943 | hp1 | a0001 | c0001 | t0004 | g0003 | AMR | PEL | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| HG01943 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | PEL | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| HG01975 | hp1 | a0002 | c0002 | t0003 | g0004 | AMR | PEL | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| HG01975 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | PEL | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| HG01978 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | PEL | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| HG01978 | hp2 | a0002 | c0002 | t0001 | g0020 | AMR | PEL | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0035 | AMR | PEL | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| HG01981 | hp2 | a0002 | c0002 | t0003 | g0061 | AMR | PEL | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| HG01993 | hp1 | a0002 | c0002 | t0001 | g0001 | AMR | PEL | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| HG01993 | hp2 | a0001 | c0001 | t0002 | g0144 | AMR | PEL | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| HG02015 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | KHV | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| HG02015 | hp2 | a0002 | c0002 | t0003 | g0004 | EAS | KHV | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| HG02055 | hp1 | a0002 | c0002 | t0003 | g0069 | AFR | ACB | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| HG02055 | hp2 | a0001 | c0001 | t0009 | g0023 | AFR | ACB | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| HG02056 | hp1 | a0001 | c0001 | t0002 | g0013 | EAS | KHV | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| HG02056 | hp2 | a0002 | c0002 | t0003 | g0004 | EAS | KHV | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| HG02071 | hp1 | a0002 | c0002 | t0001 | g0009 | EAS | KHV | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| HG02071 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | KHV | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| HG02074 | hp1 | a0001 | c0001 | t0005 | g0006 | EAS | KHV | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| HG02074 | hp2 | a0001 | c0001 | t0002 | g0016 | EAS | KHV | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| HG02080 | hp1 | a0002 | c0002 | t0001 | g0083 | EAS | KHV | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| HG02080 | hp2 | a0002 | c0002 | t0003 | g0052 | EAS | KHV | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| HG02083 | hp1 | a0001 | c0001 | t0004 | g0003 | EAS | KHV | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| HG02083 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | KHV | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| HG02129 | hp1 | a0002 | c0002 | t0003 | g0004 | EAS | KHV | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| HG02129 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | KHV | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| HG02135 | hp1 | a0002 | c0002 | t0001 | g0074 | EAS | KHV | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| HG02135 | hp2 | a0001 | c0001 | t0004 | g0003 | EAS | KHV | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| HG02145 | hp1 | a0001 | c0001 | t0005 | g0006 | AFR | ACB | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| HG02145 | hp2 | a0001 | c0001 | t0004 | g0120 | AFR | ACB | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| HG02155 | hp1 | a0001 | c0001 | t0004 | g0003 | EAS | CDX | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| HG02155 | hp2 | a0002 | c0002 | t0001 | g0084 | EAS | CDX | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| HG02257 | hp1 | a0001 | c0001 | t0008 | g0007 | AFR | ACB | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| HG02257 | hp2 | a0001 | c0001 | t0007 | g0014 | AFR | ACB | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| HG02258 | hp1 | a0001 | c0001 | t0011 | g0017 | AFR | ACB | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| HG02258 | hp2 | a0001 | c0015 | t0003 | g0159 | AFR | ACB | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| HG02273 | hp1 | a0001 | c0001 | t0004 | g0003 | AMR | PEL | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| HG02273 | hp2 | a0001 | c0001 | t0002 | g0142 | AMR | PEL | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| HG02280 | hp1 | a0001 | c0001 | t0003 | g0099 | AFR | ACB | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| HG02280 | hp2 | a0001 | c0001 | t0006 | g0030 | AFR | ACB | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| HG02293 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | PEL | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| HG02293 | hp2 | a0001 | c0001 | t0004 | g0121 | AMR | PEL | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| HG02300 | hp1 | a0001 | c0001 | t0003 | g0005 | AMR | PEL | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| HG02300 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | PEL | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| HG02451 | hp1 | a0001 | c0001 | t0008 | g0007 | AFR | ACB | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| HG02451 | hp2 | a0001 | c0001 | t0004 | g0135 | AFR | ACB | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| HG02523 | hp1 | a0001 | c0001 | t0002 | g0124 | EAS | KHV | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| HG02523 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | KHV | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| HG02572 | hp1 | a0001 | c0001 | t0010 | g0010 | AFR | GWD | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| HG02572 | hp2 | a0001 | c0001 | t0007 | g0161 | AFR | GWD | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| HG02602 | hp1 | a0002 | c0002 | t0001 | g0048 | SAS | PJL | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| HG02602 | hp2 | a0002 | c0002 | t0003 | g0004 | SAS | PJL | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| HG02622 | hp1 | a0001 | c0001 | t0005 | g0011 | AFR | GWD | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| HG02622 | hp2 | a0001 | c0001 | t0011 | g0151 | AFR | GWD | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| HG02630 | hp1 | a0001 | c0001 | t0007 | g0014 | AFR | GWD | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| HG02630 | hp2 | a0002 | c0002 | t0001 | g0009 | AFR | GWD | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| HG02647 | hp1 | a0001 | c0001 | t0013 | g0127 | AFR | GWD | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| HG02647 | hp2 | a0001 | c0001 | t0003 | g0134 | AFR | GWD | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| HG02698 | hp1 | a0002 | c0002 | t0001 | g0001 | SAS | PJL | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| HG02698 | hp2 | a0001 | c0001 | t0003 | g0005 | SAS | PJL | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| HG02717 | hp1 | a0001 | c0001 | t0020 | g0115 | AFR | GWD | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| HG02717 | hp2 | a0001 | c0001 | t0007 | g0162 | AFR | GWD | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| HG02723 | hp1 | a0001 | c0001 | t0009 | g0021 | AFR | GWD | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| HG02723 | hp2 | a0001 | c0001 | t0008 | g0113 | AFR | GWD | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| HG02735 | hp1 | a0001 | c0001 | t0002 | g0152 | SAS | PJL | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| HG02735 | hp2 | a0002 | c0002 | t0001 | g0001 | SAS | PJL | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| HG02738 | hp1 | a0002 | c0002 | t0003 | g0049 | SAS | PJL | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| HG02738 | hp2 | a0001 | c0001 | t0003 | g0005 | SAS | PJL | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| HG02809 | hp1 | a0001 | c0001 | t0021 | g0108 | AFR | GWD | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| HG02809 | hp2 | a0001 | c0001 | t0006 | g0030 | AFR | GWD | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| HG02818 | hp1 | a0002 | c0002 | t0003 | g0056 | AFR | GWD | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| HG02818 | hp2 | a0001 | c0001 | t0009 | g0130 | AFR | GWD | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| HG02886 | hp1 | a0001 | c0001 | t0009 | g0023 | AFR | GWD | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| HG02886 | hp2 | a0001 | c0001 | t0007 | g0014 | AFR | GWD | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| HG02895 | hp1 | a0001 | c0001 | t0007 | g0018 | AFR | GWD | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| HG02895 | hp2 | a0001 | c0001 | t0008 | g0007 | AFR | GWD | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| HG02896 | hp1 | a0001 | c0001 | t0008 | g0105 | AFR | GWD | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| HG02896 | hp2 | a0001 | c0001 | t0005 | g0011 | AFR | GWD | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| HG02897 | hp1 | a0001 | c0001 | t0007 | g0018 | AFR | GWD | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| HG02897 | hp2 | a0001 | c0001 | t0005 | g0011 | AFR | GWD | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| HG02922 | hp1 | a0001 | c0001 | t0007 | g0018 | AFR | ESN | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| HG02922 | hp2 | a0001 | c0001 | t0006 | g0031 | AFR | ESN | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| HG02965 | hp1 | a0001 | c0001 | t0009 | g0132 | AFR | ESN | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| HG02965 | hp2 | a0001 | c0001 | t0029 | g0106 | AFR | ESN | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| HG02970 | hp1 | a0001 | c0001 | t0007 | g0018 | AFR | ESN | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| HG02970 | hp2 | a0001 | c0001 | t0006 | g0110 | AFR | ESN | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| HG02976 | hp1 | a0001 | c0001 | t0008 | g0007 | AFR | ESN | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| HG02976 | hp2 | a0001 | c0001 | t0012 | g0154 | AFR | ESN | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| HG03017 | hp1 | a0002 | c0002 | t0001 | g0077 | SAS | PJL | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| HG03017 | hp2 | a0001 | c0001 | t0002 | g0153 | SAS | PJL | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| HG03041 | hp1 | a0001 | c0001 | t0007 | g0160 | AFR | GWD | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| HG03041 | hp2 | a0001 | c0001 | t0016 | g0109 | AFR | GWD | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| HG03098 | hp1 | a0001 | c0001 | t0011 | g0155 | AFR | MSL | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| HG03098 | hp2 | a0001 | c0001 | t0012 | g0114 | AFR | MSL | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| HG03130 | hp1 | a0001 | c0001 | t0010 | g0010 | AFR | ESN | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| HG03130 | hp2 | a0001 | c0001 | t0007 | g0014 | AFR | ESN | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| HG03139 | hp1 | a0001 | c0001 | t0003 | g0039 | AFR | ESN | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| HG03139 | hp2 | a0001 | c0001 | t0004 | g0003 | AFR | ESN | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| HG03195 | hp1 | a0001 | c0001 | t0003 | g0039 | AFR | ESN | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| HG03195 | hp2 | a0001 | c0001 | t0010 | g0010 | AFR | ESN | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| HG03209 | hp1 | a0001 | c0001 | t0030 | g0102 | AFR | MSL | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| HG03209 | hp2 | a0004 | c0006 | t0006 | g0101 | AFR | MSL | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| HG03239 | hp1 | a0007 | c0012 | t0003 | g0156 | SAS | PJL | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| HG03239 | hp2 | a0002 | c0002 | t0001 | g0019 | SAS | PJL | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| HG03486 | hp1 | a0001 | c0014 | t0006 | g0111 | AFR | MSL | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| HG03486 | hp2 | a0008 | c0011 | t0004 | g0122 | AFR | MSL | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| HG03491 | hp1 | a0002 | c0002 | t0026 | g0063 | SAS | PJL | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| HG03491 | hp2 | a0003 | c0004 | t0014 | g0025 | SAS | PJL | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| HG03492 | hp1 | a0003 | c0004 | t0014 | g0025 | SAS | PJL | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| HG03492 | hp2 | a0002 | c0002 | t0001 | g0009 | SAS | PJL | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| HG03516 | hp1 | a0001 | c0001 | t0010 | g0010 | AFR | ESN | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| HG03516 | hp2 | a0001 | c0001 | t0011 | g0017 | AFR | ESN | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| HG03540 | hp1 | a0001 | c0001 | t0008 | g0007 | AFR | GWD | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| HG03540 | hp2 | a0001 | c0001 | t0012 | g0044 | AFR | GWD | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| HG03579 | hp1 | a0002 | c0002 | t0003 | g0050 | AFR | MSL | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| HG03579 | hp2 | a0001 | c0001 | t0005 | g0011 | AFR | MSL | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| HG03654 | hp1 | a0001 | c0001 | t0004 | g0038 | SAS | PJL | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| HG03654 | hp2 | a0002 | c0002 | t0003 | g0070 | SAS | PJL | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| HG03669 | hp1 | a0002 | c0002 | t0005 | g0071 | SAS | PJL | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| HG03669 | hp2 | a0002 | c0002 | t0003 | g0004 | SAS | PJL | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| HG03688 | hp1 | a0002 | c0002 | t0003 | g0004 | SAS | STU | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| HG03688 | hp2 | a0001 | c0001 | t0002 | g0041 | SAS | STU | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| HG03704 | hp1 | a0002 | c0002 | t0003 | g0004 | SAS | PJL | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| HG03704 | hp2 | a0002 | c0002 | t0001 | g0027 | SAS | PJL | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| HG03831 | hp1 | a0002 | c0002 | t0003 | g0004 | SAS | BEB | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| HG03831 | hp2 | a0002 | c0002 | t0001 | g0027 | SAS | BEB | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| HG03834 | hp1 | a0001 | c0001 | t0004 | g0003 | SAS | BEB | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| HG03834 | hp2 | a0002 | c0002 | t0003 | g0004 | SAS | BEB | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| HG03942 | hp1 | a0002 | c0002 | t0001 | g0051 | SAS | BEB | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| HG03942 | hp2 | a0001 | c0001 | t0003 | g0005 | SAS | BEB | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| HG04115 | hp1 | a0001 | c0001 | t0003 | g0005 | SAS | STU | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| HG04115 | hp2 | a0003 | c0004 | t0001 | g0081 | SAS | STU | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| HG04184 | hp1 | a0002 | c0002 | t0035 | g0065 | SAS | BEB | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| HG04184 | hp2 | a0002 | c0002 | t0003 | g0057 | SAS | BEB | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| HG04199 | hp1 | a0001 | c0001 | t0005 | g0006 | SAS | STU | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| HG04199 | hp2 | a0002 | c0002 | t0001 | g0090 | SAS | STU | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| HG04204 | hp1 | a0002 | c0002 | t0001 | g0089 | SAS | STU | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| HG04204 | hp2 | a0001 | c0001 | t0003 | g0005 | SAS | STU | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| HG04228 | hp1 | a0002 | c0002 | t0003 | g0004 | SAS | STU | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| HG04228 | hp2 | a0001 | c0001 | t0003 | g0005 | SAS | STU | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| NA18522 | hp1 | a0001 | c0001 | t0009 | g0021 | AFR | YRI | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| NA18522 | hp2 | a0001 | c0001 | t0010 | g0010 | AFR | YRI | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| NA18612 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | CHB | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| NA18612 | hp2 | a0002 | c0002 | t0003 | g0058 | EAS | CHB | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| NA18747 | hp1 | a0001 | c0001 | t0002 | g0147 | EAS | CHB | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| NA18747 | hp2 | a0001 | c0001 | t0002 | g0016 | EAS | CHB | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| NA18906 | hp1 | a0001 | c0001 | t0033 | g0104 | AFR | YRI | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| NA18906 | hp2 | a0001 | c0001 | t0012 | g0044 | AFR | YRI | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| NA18939 | hp1 | a0001 | c0001 | t0004 | g0117 | EAS | JPT | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| NA18939 | hp2 | a0002 | c0002 | t0001 | g0075 | EAS | JPT | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| NA18940 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| NA18940 | hp2 | a0001 | c0001 | t0004 | g0003 | EAS | JPT | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| NA18941 | hp1 | a0001 | c0001 | t0004 | g0119 | EAS | JPT | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| NA18941 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| NA18942 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| NA18942 | hp2 | a0005 | c0005 | t0032 | g0097 | EAS | JPT | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| NA18943 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| NA18943 | hp2 | a0001 | c0001 | t0004 | g0003 | EAS | JPT | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| NA18944 | hp1 | a0001 | c0001 | t0004 | g0003 | EAS | JPT | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| NA18944 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| NA18946 | hp1 | a0001 | c0003 | t0004 | g0047 | EAS | JPT | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| NA18946 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| NA18947 | hp1 | a0001 | c0001 | t0004 | g0003 | EAS | JPT | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| NA18947 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| NA18948 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| NA18948 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| NA18949 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| NA18949 | hp2 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| NA18952 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| NA18952 | hp2 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| NA18954 | hp1 | a0001 | c0001 | t0004 | g0003 | EAS | JPT | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| NA18954 | hp2 | a0002 | c0002 | t0024 | g0085 | EAS | JPT | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| NA18957 | hp1 | a0002 | c0002 | t0023 | g0053 | EAS | JPT | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| NA18957 | hp2 | a0001 | c0001 | t0002 | g0140 | EAS | JPT | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| NA18961 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| NA18961 | hp2 | a0001 | c0001 | t0004 | g0003 | EAS | JPT | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| NA18962 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| NA18962 | hp2 | a0001 | c0001 | t0005 | g0006 | EAS | JPT | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| NA18963 | hp1 | a0001 | c0001 | t0004 | g0032 | EAS | JPT | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| NA18963 | hp2 | a0001 | c0001 | t0002 | g0149 | EAS | JPT | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| NA18964 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| NA18964 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| NA18965 | hp1 | a0001 | c0001 | t0002 | g0016 | EAS | JPT | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| NA18965 | hp2 | a0001 | c0001 | t0004 | g0032 | EAS | JPT | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| NA18966 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| NA18966 | hp2 | a0002 | c0002 | t0003 | g0055 | EAS | JPT | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| NA18967 | hp1 | a0001 | c0001 | t0002 | g0043 | EAS | JPT | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| NA18967 | hp2 | a0005 | c0005 | t0004 | g0096 | EAS | JPT | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| NA18968 | hp1 | a0002 | c0002 | t0001 | g0029 | EAS | JPT | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| NA18968 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| NA18970 | hp1 | a0001 | c0001 | t0004 | g0003 | EAS | JPT | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| NA18970 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| NA18971 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| NA18971 | hp2 | a0002 | c0008 | t0001 | g0087 | EAS | JPT | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| NA18972 | hp1 | a0001 | c0001 | t0004 | g0003 | EAS | JPT | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| NA18972 | hp2 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| NA18974 | hp1 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| NA18974 | hp2 | a0002 | c0002 | t0001 | g0092 | EAS | JPT | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| NA18975 | hp1 | a0001 | c0001 | t0002 | g0013 | EAS | JPT | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| NA18975 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| NA18977 | hp1 | a0001 | c0001 | t0002 | g0024 | EAS | JPT | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| NA18977 | hp2 | a0002 | c0002 | t0037 | g0066 | EAS | JPT | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| NA18978 | hp1 | a0001 | c0001 | t0004 | g0003 | EAS | JPT | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| NA18978 | hp2 | a0001 | c0001 | t0002 | g0024 | EAS | JPT | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| NA18980 | hp1 | a0001 | c0001 | t0005 | g0138 | EAS | JPT | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| NA18980 | hp2 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| NA18981 | hp1 | a0001 | c0001 | t0027 | g0123 | EAS | JPT | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| NA18981 | hp2 | a0002 | c0002 | t0001 | g0015 | EAS | JPT | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| NA18982 | hp1 | a0001 | c0001 | t0028 | g0148 | EAS | JPT | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| NA18982 | hp2 | a0002 | c0002 | t0001 | g0078 | EAS | JPT | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| NA18986 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| NA18986 | hp2 | a0001 | c0007 | t0001 | g0158 | EAS | JPT | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| NA18987 | hp1 | a0001 | c0001 | t0004 | g0003 | EAS | JPT | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| NA18987 | hp2 | a0002 | c0002 | t0003 | g0054 | EAS | JPT | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| NA18989 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| NA18989 | hp2 | a0002 | c0009 | t0001 | g0094 | EAS | JPT | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| NA18991 | hp1 | a0002 | c0002 | t0003 | g0059 | EAS | JPT | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| NA18991 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| NA18992 | hp1 | a0001 | c0001 | t0005 | g0040 | EAS | JPT | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| NA18992 | hp2 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| NA18993 | hp1 | a0001 | c0001 | t0002 | g0016 | EAS | JPT | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| NA18993 | hp2 | a0001 | c0001 | t0004 | g0118 | EAS | JPT | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| NA18994 | hp1 | a0002 | c0002 | t0003 | g0004 | EAS | JPT | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| NA18994 | hp2 | a0001 | c0001 | t0004 | g0003 | EAS | JPT | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| NA18998 | hp1 | a0002 | c0002 | t0003 | g0004 | EAS | JPT | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| NA18998 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| NA19000 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| NA19000 | hp2 | a0001 | c0007 | t0034 | g0157 | EAS | JPT | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| NA19002 | hp1 | a0001 | c0001 | t0002 | g0139 | EAS | JPT | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| NA19002 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| NA19007 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| NA19007 | hp2 | a0002 | c0002 | t0001 | g0076 | EAS | JPT | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| NA19009 | hp1 | a0002 | c0002 | t0003 | g0004 | EAS | JPT | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| NA19009 | hp2 | a0002 | c0002 | t0001 | g0093 | EAS | JPT | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| NA19012 | hp1 | a0002 | c0002 | t0001 | g0009 | EAS | JPT | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| NA19012 | hp2 | a0001 | c0001 | t0017 | g0036 | EAS | JPT | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| NA19030 | hp1 | a0001 | c0001 | t0013 | g0037 | AFR | LWK | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| NA19030 | hp2 | a0009 | c0010 | t0006 | g0095 | AFR | LWK | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| NA19043 | hp1 | a0002 | c0002 | t0012 | g0064 | AFR | LWK | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| NA19043 | hp2 | a0001 | c0001 | t0006 | g0031 | AFR | LWK | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| NA19054 | hp1 | a0001 | c0001 | t0002 | g0013 | EAS | JPT | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| NA19054 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| NA19055 | hp1 | a0002 | c0002 | t0003 | g0004 | EAS | JPT | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| NA19055 | hp2 | a0001 | c0001 | t0004 | g0003 | EAS | JPT | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| NA19058 | hp1 | a0002 | c0002 | t0001 | g0029 | EAS | JPT | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| NA19058 | hp2 | a0001 | c0001 | t0005 | g0040 | EAS | JPT | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| NA19060 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| NA19060 | hp2 | a0002 | c0002 | t0001 | g0015 | EAS | JPT | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| NA19062 | hp1 | a0002 | c0002 | t0001 | g0015 | EAS | JPT | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| NA19062 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| NA19063 | hp1 | a0002 | c0002 | t0003 | g0004 | EAS | JPT | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| NA19063 | hp2 | a0001 | c0003 | t0004 | g0026 | EAS | JPT | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| NA19064 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| NA19064 | hp2 | a0002 | c0002 | t0003 | g0004 | EAS | JPT | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| NA19065 | hp1 | a0001 | c0001 | t0004 | g0003 | EAS | JPT | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| NA19065 | hp2 | a0002 | c0002 | t0001 | g0082 | EAS | JPT | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| NA19067 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| NA19067 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| NA19070 | hp1 | a0001 | c0001 | t0002 | g0146 | EAS | JPT | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| NA19070 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| NA19074 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| NA19074 | hp2 | a0001 | c0001 | t0002 | g0013 | EAS | JPT | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| NA19075 | hp1 | a0002 | c0002 | t0001 | g0091 | EAS | JPT | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| NA19075 | hp2 | a0001 | c0001 | t0015 | g0034 | EAS | JPT | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| NA19076 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| NA19076 | hp2 | a0001 | c0001 | t0004 | g0033 | EAS | JPT | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| NA19077 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| NA19077 | hp2 | a0002 | c0002 | t0003 | g0004 | EAS | JPT | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| NA19079 | hp1 | a0002 | c0002 | t0003 | g0004 | EAS | JPT | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| NA19079 | hp2 | a0001 | c0001 | t0002 | g0145 | EAS | JPT | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| NA19080 | hp1 | a0001 | c0001 | t0015 | g0034 | EAS | JPT | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| NA19080 | hp2 | a0001 | c0001 | t0002 | g0141 | EAS | JPT | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| NA19083 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| NA19083 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| NA19084 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| NA19084 | hp2 | a0002 | c0002 | t0001 | g0062 | EAS | JPT | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| NA19085 | hp1 | a0002 | c0002 | t0001 | g0088 | EAS | JPT | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| NA19085 | hp2 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| NA19086 | hp1 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| NA19086 | hp2 | a0002 | c0002 | t0001 | g0019 | EAS | JPT | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| NA19087 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| NA19087 | hp2 | a0001 | c0001 | t0002 | g0013 | EAS | JPT | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| NA19088 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| NA19088 | hp2 | a0001 | c0001 | t0004 | g0033 | EAS | JPT | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| NA19090 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| NA19090 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| NA19091 | hp1 | a0001 | c0001 | t0017 | g0036 | EAS | JPT | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| NA19091 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| NA19240 | hp1 | a0001 | c0001 | t0008 | g0007 | AFR | YRI | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| NA19240 | hp2 | a0002 | c0002 | t0038 | g0164 | AFR | YRI | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| NA20129 | hp1 | a0001 | c0001 | t0011 | g0017 | AFR | ASW | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| NA20129 | hp2 | a0001 | c0001 | t0005 | g0011 | AFR | ASW | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| NA20752 | hp1 | a0001 | c0001 | t0003 | g0005 | EUR | TSI | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| NA20752 | hp2 | a0002 | c0002 | t0001 | g0009 | EUR | TSI | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| NA20805 | hp1 | a0002 | c0002 | t0003 | g0004 | EUR | TSI | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| NA20805 | hp2 | a0001 | c0001 | t0004 | g0003 | EUR | TSI | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| NA20905 | hp1 | a0002 | c0002 | t0001 | g0079 | SAS | GIH | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| NA20905 | hp2 | a0002 | c0002 | t0001 | g0009 | SAS | GIH | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| HG01123 | hp1 | a0002 | c0002 | t0001 | g0009 | AMR | CLM | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| HG01123 | hp2 | a0002 | c0002 | t0003 | g0004 | AMR | CLM | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| HG02109 | hp1 | a0001 | c0001 | t0009 | g0133 | AFR | ACB | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| HG02109 | hp2 | a0001 | c0001 | t0005 | g0011 | AFR | ACB | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| HG02486 | hp1 | a0001 | c0001 | t0006 | g0112 | AFR | ACB | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| HG02486 | hp2 | a0001 | c0001 | t0010 | g0010 | AFR | ACB | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| HG02559 | hp1 | a0001 | c0001 | t0009 | g0023 | AFR | ACB | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| HG02559 | hp2 | a0001 | c0001 | t0008 | g0007 | AFR | ACB | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| HG03471 | hp1 | a0004 | c0006 | t0006 | g0100 | AFR | MSL | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| HG03471 | hp2 | a0001 | c0001 | t0013 | g0037 | AFR | MSL | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| HG06807 | hp1 | a0001 | c0001 | t0003 | g0005 | AFR | USA | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| HG06807 | hp2 | a0001 | c0001 | t0004 | g0003 | AFR | USA | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| NA18955 | hp1 | a0002 | c0002 | t0019 | g0046 | EAS | JPT | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| NA18955 | hp2 | a0001 | c0003 | t0004 | g0026 | EAS | JPT | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| NA20300 | hp1 | a0001 | c0001 | t0004 | g0003 | AFR | USA | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| NA20300 | hp2 | a0001 | c0001 | t0009 | g0021 | AFR | USA | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| NA21309 | hp1 | a0001 | c0001 | t0018 | g0045 | AFR | LWK | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| NA21309 | hp2 | a0001 | c0001 | t0022 | g0116 | AFR | LWK | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| homoSapiens | chm13v2 | a0002 | c0002 | t0003 | g0004 | REF | REF | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0004 | g0038 | REF | REF | TBX18_chr6_84727496_84769598 | TBX18 | chr6 | 84727496 | 84769598 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:84737244 | C | T | 1 | a0004 | 2 | HG03209.hp2 HG03471.hp1 |
missense_variant | MODERATE | c.1265G>A | p.Arg422His | TBX18 | ENSG00000112837.17 | transcript | ENST00000369663.10 | protein_coding | 8/8 | 1682/6430 | 1265/1824 | 422/607 | chr6 | 84737244 | |||
| chr6:84737322 | G | A | 1 | a0007 | 1 | HG03239.hp1 | missense_variant | MODERATE | c.1187C>T | p.Ser396Phe | TBX18 | ENSG00000112837.17 | transcript | ENST00000369663.10 | protein_coding | 8/8 | 1604/6430 | 1187/1824 | 396/607 | chr6 | 84737322 | |||
| chr6:84737407 | T | G | 1 | a0006 | 1 | HG00642.hp2 | missense_variant&splice_region_variant | MODERATE | c.1102A>C | p.Asn368His | TBX18 | ENSG00000112837.17 | transcript | ENST00000369663.10 | protein_coding | 8/8 | 1519/6430 | 1102/1824 | 368/607 | chr6 | 84737407 | |||
| chr6:84747991 | C | T | 1 | a0003 | 3 | HG03491.hp2 HG03492.hp1 HG04115.hp2 |
missense_variant | MODERATE | c.868G>A | p.Gly290Arg | TBX18 | ENSG00000112837.17 | transcript | ENST00000369663.10 | protein_coding | 5/8 | 1285/6430 | 868/1824 | 290/607 | chr6 | 84747991 | |||
| chr6:84748053 | C | T | 1 | a0008 | 1 | HG03486.hp2 | missense_variant | MODERATE | c.806G>A | p.Arg269Gln | TBX18 | ENSG00000112837.17 | transcript | ENST00000369663.10 | protein_coding | 5/8 | 1223/6430 | 806/1824 | 269/607 | chr6 | 84748053 | |||
| chr6:84763926 | C | CCGGCCCA others(5): Show |
1 | a0005 | 2 | NA18942.hp2 NA18967.hp2 |
conservative_inframe_insertion | MODERATE | c.244_255dupACGTCTGG others(4): Show |
p.Pro85_Ala86insThrS others(8): Show |
TBX18 | ENSG00000112837.17 | transcript | ENST00000369663.10 | protein_coding | 1/8 | 672/6430 | 255/1824 | 85/607 | chr6 | 84763926 | |||
| chr6:84763937 | G | T | 1 | a0009 | 1 | NA19030.hp2 | missense_variant | MODERATE | c.245C>A | p.Thr82Lys | TBX18 | ENSG00000112837.17 | transcript | ENST00000369663.10 | protein_coding | 1/8 | 662/6430 | 245/1824 | 82/607 | chr6 | 84763937 | |||
| chr6:84764040 | C | T | 2 | a0002 a0003 |
148 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(145): Show |
missense_variant | MODERATE | c.142G>A | p.Gly48Arg | TBX18 | ENSG00000112837.17 | transcript | ENST00000369663.10 | protein_coding | 1/8 | 559/6430 | 142/1824 | 48/607 | chr6 | 84764040 |
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:84737228 | G | C | 1 | a0002c0008 | 1 | NA18971.hp2 | synonymous_variant | LOW | c.1281C>G | p.Leu427Leu | TBX18 | ENSG00000112837.17 | transcript | ENST00000369663.10 | protein_coding | 8/8 | 1698/6430 | 1281/1824 | 427/607 | chr6 | 84737228 | |||
| chr6:84756743 | G | A | 1 | a0001c0014 | 1 | HG03486.hp1 | synonymous_variant | LOW | c.726C>T | p.Phe242Phe | TBX18 | ENSG00000112837.17 | transcript | ENST00000369663.10 | protein_coding | 4/8 | 1143/6430 | 726/1824 | 242/607 | chr6 | 84756743 | |||
| chr6:84762549 | G | A | 1 | a0001c0007 | 2 | NA18986.hp2 NA19000.hp2 |
synonymous_variant | LOW | c.492C>T | p.Ala164Ala | TBX18 | ENSG00000112837.17 | transcript | ENST00000369663.10 | protein_coding | 2/8 | 909/6430 | 492/1824 | 164/607 | chr6 | 84762549 | |||
| chr6:84762705 | C | A | 1 | a0001c0015 | 1 | HG02258.hp2 | synonymous_variant | LOW | c.336G>T | p.Ala112Ala | TBX18 | ENSG00000112837.17 | transcript | ENST00000369663.10 | protein_coding | 2/8 | 753/6430 | 336/1824 | 112/607 | chr6 | 84762705 | |||
| chr6:84763975 | T | G | 1 | a0002c0009 | 1 | NA18989.hp2 | synonymous_variant | LOW | c.207A>C | p.Gly69Gly | TBX18 | ENSG00000112837.17 | transcript | ENST00000369663.10 | protein_coding | 1/8 | 624/6430 | 207/1824 | 69/607 | chr6 | 84763975 | |||
| chr6:84764041 | C | G | 1 | a0001c0003 | 3 | NA18946.hp1 NA18955.hp2 NA19063.hp2 |
synonymous_variant | LOW | c.141G>C | p.Ala47Ala | TBX18 | ENSG00000112837.17 | transcript | ENST00000369663.10 | protein_coding | 1/8 | 558/6430 | 141/1824 | 47/607 | chr6 | 84764041 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:84732820 | G | GTA | 10 | a0001c0001t0005 a0001c0001t0007 a0001c0001t0008 others(7): Show |
66 | HG00099.hp2 HG00639.hp2 HG00741.hp2 others(63): Show |
3_prime_UTR_variant | MODIFIER | c.*3863_*3864dupTA | TBX18 | ENSG00000112837.17 | transcript | ENST00000369663.10 | protein_coding | 8/8 | 3864 | chr6 | 84732820 | ||||||
| chr6:84732820 | GTA | G | 8 | a0001c0001t0003 a0001c0001t0012 a0001c0015t0003 others(5): Show |
70 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(67): Show |
3_prime_UTR_variant | MODIFIER | c.*3863_*3864delTA | TBX18 | ENSG00000112837.17 | transcript | ENST00000369663.10 | protein_coding | 8/8 | 3863 | chr6 | 84732820 | ||||||
| chr6:84733050 | T | C | 1 | a0001c0001t0028 | 1 | NA18982.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3635A>G | TBX18 | ENSG00000112837.17 | transcript | ENST00000369663.10 | protein_coding | 8/8 | 3635 | chr6 | 84733050 | ||||||
| chr6:84733173 | T | A | 1 | a0006c0013t0036 | 1 | HG00642.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3512A>T | TBX18 | ENSG00000112837.17 | transcript | ENST00000369663.10 | protein_coding | 8/8 | 3512 | chr6 | 84733173 | ||||||
| chr6:84733247 | G | C | 1 | a0001c0001t0029 | 1 | HG02965.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3438C>G | TBX18 | ENSG00000112837.17 | transcript | ENST00000369663.10 | protein_coding | 8/8 | 3438 | chr6 | 84733247 | ||||||
| chr6:84733264 | A | T | 3 | a0001c0001t0012 a0002c0002t0012 a0002c0002t0035 |
7 | HG01884.hp1 HG02976.hp2 HG03098.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*3421T>A | TBX18 | ENSG00000112837.17 | transcript | ENST00000369663.10 | protein_coding | 8/8 | 3421 | chr6 | 84733264 | ||||||
| chr6:84733306 | T | C | 1 | a0001c0001t0009 | 10 | HG01884.hp2 HG02055.hp2 HG02109.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*3379A>G | TBX18 | ENSG00000112837.17 | transcript | ENST00000369663.10 | protein_coding | 8/8 | 3379 | chr6 | 84733306 | ||||||
| chr6:84733405 | A | C | 1 | a0001c0001t0015 | 2 | NA19075.hp2 NA19080.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3280T>G | TBX18 | ENSG00000112837.17 | transcript | ENST00000369663.10 | protein_coding | 8/8 | 3280 | chr6 | 84733405 | ||||||
| chr6:84733411 | T | C | 1 | a0001c0001t0030 | 1 | HG03209.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3274A>G | TBX18 | ENSG00000112837.17 | transcript | ENST00000369663.10 | protein_coding | 8/8 | 3274 | chr6 | 84733411 | ||||||
| chr6:84733678 | C | T | 1 | a0001c0001t0022 | 1 | NA21309.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3007G>A | TBX18 | ENSG00000112837.17 | transcript | ENST00000369663.10 | protein_coding | 8/8 | 3007 | chr6 | 84733678 | ||||||
| chr6:84733745 | A | G | 1 | a0001c0001t0013 | 3 | HG02647.hp1 HG03471.hp2 NA19030.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2940T>C | TBX18 | ENSG00000112837.17 | transcript | ENST00000369663.10 | protein_coding | 8/8 | 2940 | chr6 | 84733745 | ||||||
| chr6:84733865 | T | A | 1 | a0001c0001t0011 | 6 | HG01109.hp2 HG02258.hp1 HG02622.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*2820A>T | TBX18 | ENSG00000112837.17 | transcript | ENST00000369663.10 | protein_coding | 8/8 | 2820 | chr6 | 84733865 | ||||||
| chr6:84733931 | T | C | 13 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0011 others(10): Show |
154 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(151): Show |
3_prime_UTR_variant | MODIFIER | c.*2754A>G | TBX18 | ENSG00000112837.17 | transcript | ENST00000369663.10 | protein_coding | 8/8 | 2754 | chr6 | 84733931 | ||||||
| chr6:84734138 | C | T | 9 | a0001c0001t0006 a0001c0001t0018 a0001c0001t0021 others(6): Show |
19 | HG01106.hp1 HG01243.hp2 HG01516.hp1 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*2547G>A | TBX18 | ENSG00000112837.17 | transcript | ENST00000369663.10 | protein_coding | 8/8 | 2547 | chr6 | 84734138 | ||||||
| chr6:84734194 | C | T | 1 | a0001c0001t0028 | 1 | NA18982.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2491G>A | TBX18 | ENSG00000112837.17 | transcript | ENST00000369663.10 | protein_coding | 8/8 | 2491 | chr6 | 84734194 | ||||||
| chr6:84734247 | A | G | 1 | a0001c0001t0027 | 1 | NA18981.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2438T>C | TBX18 | ENSG00000112837.17 | transcript | ENST00000369663.10 | protein_coding | 8/8 | 2438 | chr6 | 84734247 | ||||||
| chr6:84734371 | G | A | 44 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(41): Show |
340 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(337): Show |
3_prime_UTR_variant | MODIFIER | c.*2314C>T | TBX18 | ENSG00000112837.17 | transcript | ENST00000369663.10 | protein_coding | 8/8 | 2314 | chr6 | 84734371 | ||||||
| chr6:84734905 | T | G | 1 | a0002c0002t0031 | 1 | HG00597.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1780A>C | TBX18 | ENSG00000112837.17 | transcript | ENST00000369663.10 | protein_coding | 8/8 | 1780 | chr6 | 84734905 | ||||||
| chr6:84734907 | C | T | 1 | a0001c0001t0025 | 1 | HG00423.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1778G>A | TBX18 | ENSG00000112837.17 | transcript | ENST00000369663.10 | protein_coding | 8/8 | 1778 | chr6 | 84734907 | ||||||
| chr6:84734948 | G | T | 1 | a0002c0002t0024 | 1 | NA18954.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1737C>A | TBX18 | ENSG00000112837.17 | transcript | ENST00000369663.10 | protein_coding | 8/8 | 1737 | chr6 | 84734948 | ||||||
| chr6:84735508 | A | G | 1 | a0001c0001t0020 | 1 | HG02717.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1177T>C | TBX18 | ENSG00000112837.17 | transcript | ENST00000369663.10 | protein_coding | 8/8 | 1177 | chr6 | 84735508 | ||||||
| chr6:84735549 | T | C | 1 | a0005c0005t0032 | 1 | NA18942.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1136A>G | TBX18 | ENSG00000112837.17 | transcript | ENST00000369663.10 | protein_coding | 8/8 | 1136 | chr6 | 84735549 | ||||||
| chr6:84735686 | C | T | 1 | a0002c0002t0023 | 1 | NA18957.hp1 | 3_prime_UTR_variant | MODIFIER | c.*999G>A | TBX18 | ENSG00000112837.17 | transcript | ENST00000369663.10 | protein_coding | 8/8 | 999 | chr6 | 84735686 | ||||||
| chr6:84735742 | T | C | 5 | a0001c0001t0008 a0001c0001t0010 a0001c0001t0013 others(2): Show |
22 | HG01891.hp1 HG01891.hp2 HG02257.hp1 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*943A>G | TBX18 | ENSG00000112837.17 | transcript | ENST00000369663.10 | protein_coding | 8/8 | 943 | chr6 | 84735742 | ||||||
| chr6:84735934 | T | C | 1 | a0001c0001t0033 | 1 | NA18906.hp1 | 3_prime_UTR_variant | MODIFIER | c.*751A>G | TBX18 | ENSG00000112837.17 | transcript | ENST00000369663.10 | protein_coding | 8/8 | 751 | chr6 | 84735934 | ||||||
| chr6:84736000 | T | G | 1 | a0001c0007t0034 | 1 | NA19000.hp2 | 3_prime_UTR_variant | MODIFIER | c.*685A>C | TBX18 | ENSG00000112837.17 | transcript | ENST00000369663.10 | protein_coding | 8/8 | 685 | chr6 | 84736000 | ||||||
| chr6:84736216 | C | T | 1 | a0001c0001t0022 | 1 | NA21309.hp2 | 3_prime_UTR_variant | MODIFIER | c.*469G>A | TBX18 | ENSG00000112837.17 | transcript | ENST00000369663.10 | protein_coding | 8/8 | 469 | chr6 | 84736216 | ||||||
| chr6:84736293 | T | A | 3 | a0001c0001t0012 a0002c0002t0012 a0002c0002t0035 |
7 | HG01884.hp1 HG02976.hp2 HG03098.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*392A>T | TBX18 | ENSG00000112837.17 | transcript | ENST00000369663.10 | protein_coding | 8/8 | 392 | chr6 | 84736293 | ||||||
| chr6:84736419 | A | G | 6 | a0001c0001t0007 a0001c0001t0008 a0001c0001t0010 others(3): Show |
34 | HG00741.hp2 HG01891.hp1 HG01891.hp2 others(31): Show |
3_prime_UTR_variant | MODIFIER | c.*266T>C | TBX18 | ENSG00000112837.17 | transcript | ENST00000369663.10 | protein_coding | 8/8 | 266 | chr6 | 84736419 | ||||||
| chr6:84736423 | G | A | 1 | a0001c0001t0013 | 3 | HG02647.hp1 HG03471.hp2 NA19030.hp1 |
3_prime_UTR_variant | MODIFIER | c.*262C>T | TBX18 | ENSG00000112837.17 | transcript | ENST00000369663.10 | protein_coding | 8/8 | 262 | chr6 | 84736423 | ||||||
| chr6:84736454 | CAG | C | 2 | a0001c0001t0016 a0006c0013t0036 |
3 | HG00642.hp2 HG01109.hp1 HG03041.hp2 |
3_prime_UTR_variant | MODIFIER | c.*229_*230delCT | TBX18 | ENSG00000112837.17 | transcript | ENST00000369663.10 | protein_coding | 8/8 | 229 | chr6 | 84736454 | ||||||
| chr6:84736468 | G | A | 1 | a0002c0002t0037 | 1 | NA18977.hp2 | 3_prime_UTR_variant | MODIFIER | c.*217C>T | TBX18 | ENSG00000112837.17 | transcript | ENST00000369663.10 | protein_coding | 8/8 | 217 | chr6 | 84736468 | ||||||
| chr6:84736603 | G | C | 2 | a0001c0001t0008 a0001c0001t0017 |
13 | HG01891.hp1 HG01891.hp2 HG02257.hp1 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*82C>G | TBX18 | ENSG00000112837.17 | transcript | ENST00000369663.10 | protein_coding | 8/8 | 82 | chr6 | 84736603 | ||||||
| chr6:84764182 | C | T | 1 | a0001c0001t0002 | 4 | NA18944.hp2 NA18968.hp2 NA19060.hp1 others(1): Show |
5_prime_UTR_variant | MODIFIER | c.-1G>A | TBX18 | ENSG00000112837.17 | transcript | ENST00000369663.10 | protein_coding | 1/8 | 1 | chr6 | 84764182 | ||||||
| chr6:84764199 | C | A | 1 | a0002c0002t0038 | 1 | NA19240.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-18G>T | TBX18 | ENSG00000112837.17 | transcript | ENST00000369663.10 | protein_coding | 1/8 | chr6 | 84764199 | |||||||
| chr6:84764346 | C | G | 1 | a0003c0004t0014 | 2 | HG03491.hp2 HG03492.hp1 |
5_prime_UTR_variant | MODIFIER | c.-165G>C | TBX18 | ENSG00000112837.17 | transcript | ENST00000369663.10 | protein_coding | 1/8 | 165 | chr6 | 84764346 | ||||||
| chr6:84764516 | A | G | 1 | a0002c0002t0019 | 1 | NA18955.hp1 | 5_prime_UTR_variant | MODIFIER | c.-335T>C | TBX18 | ENSG00000112837.17 | transcript | ENST00000369663.10 | protein_coding | 1/8 | 335 | chr6 | 84764516 | ||||||
| chr6:84764564 | C | T | 1 | a0001c0001t0018 | 1 | NA21309.hp1 | 5_prime_UTR_variant | MODIFIER | c.-383G>A | TBX18 | ENSG00000112837.17 | transcript | ENST00000369663.10 | protein_coding | 1/8 | 383 | chr6 | 84764564 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:84737464 | A | G | 5 | a0001c0001t0010g0010 a0001c0001t0013g0037 a0001c0001t0013g0127 others(2): Show |
11 | HG02486.hp2 HG02572.hp1 HG02647.hp1 others(8): Show |
intron_variant | MODIFIER | c.1100-55T>C | TBX18 | ENSG00000112837.17 | transcript | ENST00000369663.10 | protein_coding | 7/7 | chr6 | 84737464 | |||||||
| chr6:84737667 | G | C | 1 | a0001c0001t0009g0132 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1100-258C>G | TBX18 | ENSG00000112837.17 | transcript | ENST00000369663.10 | protein_coding | 7/7 | chr6 | 84737667 | |||||||
| chr6:84737684 | C | T | 1 | a0002c0002t0001g0048 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1100-275G>A | TBX18 | ENSG00000112837.17 | transcript | ENST00000369663.10 | protein_coding | 7/7 | chr6 | 84737684 | |||||||
| chr6:84737766 | G | A | 2 | a0002c0002t0001g0015 a0002c0008t0001g0087 |
5 | HG00609.hp2 NA18971.hp2 NA18981.hp2 others(2): Show |
intron_variant | MODIFIER | c.1100-357C>T | TBX18 | ENSG00000112837.17 | transcript | ENST00000369663.10 | protein_coding | 7/7 | chr6 | 84737766 | |||||||
| chr6:84737802 | C | T | 1 | a0002c0002t0001g0079 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1100-393G>A | TBX18 | ENSG00000112837.17 | transcript | ENST00000369663.10 | protein_coding | 7/7 | chr6 | 84737802 | |||||||
| chr6:84737941 | A | G | 1 | a0002c0002t0001g0084 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.1100-532T>C | TBX18 | ENSG00000112837.17 | transcript | ENST00000369663.10 | protein_coding | 7/7 | chr6 | 84737941 | |||||||
| chr6:84737998 | T | C | 1 | a0002c0009t0001g0094 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.1099+499A>G | TBX18 | ENSG00000112837.17 | transcript | ENST00000369663.10 | protein_coding | 7/7 | chr6 | 84737998 | |||||||
| chr6:84738113 | G | A | 5 | a0001c0001t0008g0007 a0001c0001t0008g0098 a0001c0001t0008g0105 others(2): Show |
12 | HG01891.hp1 HG01891.hp2 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.1099+384C>T | TBX18 | ENSG00000112837.17 | transcript | ENST00000369663.10 | protein_coding | 7/7 | chr6 | 84738113 | |||||||
| chr6:84738118 | C | T | 3 | a0001c0001t0012g0044 a0001c0001t0012g0114 a0001c0001t0012g0154 |
4 | HG02976.hp2 HG03098.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.1099+379G>A | TBX18 | ENSG00000112837.17 | transcript | ENST00000369663.10 | protein_coding | 7/7 | chr6 | 84738118 | |||||||
| chr6:84738217 | G | A | 3 | a0001c0001t0012g0044 a0001c0001t0012g0114 a0001c0001t0012g0154 |
4 | HG02976.hp2 HG03098.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.1099+280C>T | TBX18 | ENSG00000112837.17 | transcript | ENST00000369663.10 | protein_coding | 7/7 | chr6 | 84738217 | |||||||
| chr6:84738385 | C | T | 55 | a0001c0001t0002g0002 a0001c0001t0002g0008 a0001c0001t0002g0013 others(52): Show |
150 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(147): Show |
intron_variant | MODIFIER | c.1099+112G>A | TBX18 | ENSG00000112837.17 | transcript | ENST00000369663.10 | protein_coding | 7/7 | chr6 | 84738385 | |||||||
| chr6:84738468 | T | C | 1 | a0002c0002t0003g0067 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1099+29A>G | TBX18 | ENSG00000112837.17 | transcript | ENST00000369663.10 | protein_coding | 7/7 | chr6 | 84738468 | |||||||
| chr6:84738847 | A | G | 138 | a0001c0001t0002g0002 a0001c0001t0002g0008 a0001c0001t0002g0013 others(135): Show |
339 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(336): Show |
intron_variant | MODIFIER | c.1005-256T>C | TBX18 | ENSG00000112837.17 | transcript | ENST00000369663.10 | protein_coding | 6/7 | chr6 | 84738847 | |||||||
| chr6:84739351 | A | G | 8 | a0001c0001t0006g0022 a0001c0001t0006g0131 a0001c0001t0009g0021 others(5): Show |
14 | HG01106.hp1 HG01243.hp2 HG01516.hp1 others(11): Show |
intron_variant | MODIFIER | c.1005-760T>C | TBX18 | ENSG00000112837.17 | transcript | ENST00000369663.10 | protein_coding | 6/7 | chr6 | 84739351 | |||||||
| chr6:84739460 | A | C | 5 | a0001c0001t0008g0007 a0001c0001t0008g0098 a0001c0001t0008g0105 others(2): Show |
12 | HG01891.hp1 HG01891.hp2 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.1005-869T>G | TBX18 | ENSG00000112837.17 | transcript | ENST00000369663.10 | protein_coding | 6/7 | chr6 | 84739460 | |||||||
| chr6:84739548 | A | C | 2 | a0001c0001t0009g0132 a0001c0001t0009g0133 |
2 | HG02109.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.1005-957T>G | TBX18 | ENSG00000112837.17 | transcript | ENST00000369663.10 | protein_coding | 6/7 | chr6 | 84739548 | |||||||
| chr6:84739695 | T | C | 3 | a0001c0001t0012g0044 a0001c0001t0012g0114 a0001c0001t0012g0154 |
4 | HG02976.hp2 HG03098.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.1005-1104A>G | TBX18 | ENSG00000112837.17 | transcript | ENST00000369663.10 | protein_coding | 6/7 | chr6 | 84739695 | |||||||
| chr6:84739707 | G | A | 1 | a0001c0001t0005g0138 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.1005-1116C>T | TBX18 | ENSG00000112837.17 | transcript | ENST00000369663.10 | protein_coding | 6/7 | chr6 | 84739707 | |||||||
| chr6:84739813 | T | C | 2 | a0001c0007t0001g0158 a0001c0007t0034g0157 |
2 | NA18986.hp2 NA19000.hp2 |
intron_variant | MODIFIER | c.1005-1222A>G | TBX18 | ENSG00000112837.17 | transcript | ENST00000369663.10 | protein_coding | 6/7 | chr6 | 84739813 | |||||||
| chr6:84739914 | G | A | 1 | a0001c0001t0007g0161 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1005-1323C>T | TBX18 | ENSG00000112837.17 | transcript | ENST00000369663.10 | protein_coding | 6/7 | chr6 | 84739914 | |||||||
| chr6:84739935 | G | T | 5 | a0001c0001t0007g0014 a0001c0001t0007g0018 a0001c0001t0007g0160 others(2): Show |
12 | HG00741.hp2 HG02257.hp2 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.1005-1344C>A | TBX18 | ENSG00000112837.17 | transcript | ENST00000369663.10 | protein_coding | 6/7 | chr6 | 84739935 | |||||||
| chr6:84739947 | C | T | 17 | a0001c0001t0003g0099 a0001c0001t0006g0030 a0001c0001t0006g0031 others(14): Show |
19 | HG01109.hp1 HG01884.hp1 HG02280.hp1 others(16): Show |
intron_variant | MODIFIER | c.1005-1356G>A | TBX18 | ENSG00000112837.17 | transcript | ENST00000369663.10 | protein_coding | 6/7 | chr6 | 84739947 | |||||||
| chr6:84739969 | T | C | 1 | a0001c0001t0029g0106 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1005-1378A>G | TBX18 | ENSG00000112837.17 | transcript | ENST00000369663.10 | protein_coding | 6/7 | chr6 | 84739969 | |||||||
| chr6:84740302 | C | T | 3 | a0001c0001t0012g0044 a0001c0001t0012g0114 a0001c0001t0012g0154 |
4 | HG02976.hp2 HG03098.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.1005-1711G>A | TBX18 | ENSG00000112837.17 | transcript | ENST00000369663.10 | protein_coding | 6/7 | chr6 | 84740302 | |||||||
| chr6:84740437 | T | G | 1 | a0001c0001t0002g0153 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1005-1846A>C | TBX18 | ENSG00000112837.17 | transcript | ENST00000369663.10 | protein_coding | 6/7 | chr6 | 84740437 | |||||||
| chr6:84740555 | T | TGGCAGAC others(11): Show |
6 | a0001c0001t0004g0012 a0001c0001t0005g0006 a0001c0001t0005g0040 others(3): Show |
19 | HG00099.hp2 HG00639.hp2 HG01070.hp2 others(16): Show |
intron_variant | MODIFIER | c.1005-1982_1005-196 others(22): Show |
TBX18 | ENSG00000112837.17 | transcript | ENST00000369663.10 | protein_coding | 6/7 | chr6 | 84740555 | |||||||
| chr6:84740580 | A | C | 3 | a0001c0001t0012g0044 a0001c0001t0012g0114 a0001c0001t0012g0154 |
4 | HG02976.hp2 HG03098.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.1005-1989T>G | TBX18 | ENSG00000112837.17 | transcript | ENST00000369663.10 | protein_coding | 6/7 | chr6 | 84740580 | |||||||
| chr6:84740660 | T | C | 1 | a0001c0001t0002g0147 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.1005-2069A>G | TBX18 | ENSG00000112837.17 | transcript | ENST00000369663.10 | protein_coding | 6/7 | chr6 | 84740660 | |||||||
| chr6:84740971 | T | A | 1 | a0001c0001t0002g0152 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1005-2380A>T | TBX18 | ENSG00000112837.17 | transcript | ENST00000369663.10 | protein_coding | 6/7 | chr6 | 84740971 | |||||||
| chr6:84741056 | G | A | 3 | a0001c0001t0012g0044 a0001c0001t0012g0114 a0001c0001t0012g0154 |
4 | HG02976.hp2 HG03098.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.1005-2465C>T | TBX18 | ENSG00000112837.17 | transcript | ENST00000369663.10 | protein_coding | 6/7 | chr6 | 84741056 | |||||||
| chr6:84741142 | T | C | 1 | a0001c0001t0016g0107 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1005-2551A>G | TBX18 | ENSG00000112837.17 | transcript | ENST00000369663.10 | protein_coding | 6/7 | chr6 | 84741142 | |||||||
| chr6:84741144 | A | G | 3 | a0001c0001t0016g0107 a0001c0001t0016g0109 a0001c0001t0029g0106 |
3 | HG01109.hp1 HG02965.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.1005-2553T>C | TBX18 | ENSG00000112837.17 | transcript | ENST00000369663.10 | protein_coding | 6/7 | chr6 | 84741144 | |||||||
| chr6:84741249 | C | T | 1 | a0001c0001t0022g0116 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1005-2658G>A | TBX18 | ENSG00000112837.17 | transcript | ENST00000369663.10 | protein_coding | 6/7 | chr6 | 84741249 | |||||||
| chr6:84741267 | C | G | 1 | a0002c0002t0001g0083 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.1005-2676G>C | TBX18 | ENSG00000112837.17 | transcript | ENST00000369663.10 | protein_coding | 6/7 | chr6 | 84741267 | |||||||
| chr6:84741361 | T | C | 139 | a0001c0001t0002g0002 a0001c0001t0002g0008 a0001c0001t0002g0013 others(136): Show |
340 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(337): Show |
intron_variant | MODIFIER | c.1005-2770A>G | TBX18 | ENSG00000112837.17 | transcript | ENST00000369663.10 | protein_coding | 6/7 | chr6 | 84741361 | |||||||
| chr6:84741583 | C | T | 2 | a0001c0001t0003g0005 a0007c0012t0003g0156 |
11 | HG01168.hp2 HG02300.hp1 HG02698.hp2 others(8): Show |
intron_variant | MODIFIER | c.1004+2678G>A | TBX18 | ENSG00000112837.17 | transcript | ENST00000369663.10 | protein_coding | 6/7 | chr6 | 84741583 | |||||||
| chr6:84741667 | G | A | 1 | a0002c0002t0001g0088 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.1004+2594C>T | TBX18 | ENSG00000112837.17 | transcript | ENST00000369663.10 | protein_coding | 6/7 | chr6 | 84741667 | |||||||
| chr6:84741764 | C | T | 3 | a0001c0001t0012g0044 a0001c0001t0012g0114 a0001c0001t0012g0154 |
4 | HG02976.hp2 HG03098.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.1004+2497G>A | TBX18 | ENSG00000112837.17 | transcript | ENST00000369663.10 | protein_coding | 6/7 | chr6 | 84741764 | |||||||
| chr6:84741897 | C | T | 1 | a0001c0001t0005g0137 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.1004+2364G>A | TBX18 | ENSG00000112837.17 | transcript | ENST00000369663.10 | protein_coding | 6/7 | chr6 | 84741897 | |||||||
| chr6:84741959 | C | A | 2 | a0001c0001t0004g0032 a0001c0001t0004g0033 |
4 | NA18963.hp1 NA18965.hp2 NA19076.hp2 others(1): Show |
intron_variant | MODIFIER | c.1004+2302G>T | TBX18 | ENSG00000112837.17 | transcript | ENST00000369663.10 | protein_coding | 6/7 | chr6 | 84741959 | |||||||
| chr6:84742015 | G | A | 1 | a0001c0001t0006g0110 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1004+2246C>T | TBX18 | ENSG00000112837.17 | transcript | ENST00000369663.10 | protein_coding | 6/7 | chr6 | 84742015 | |||||||
| chr6:84742032 | G | A | 1 | a0002c0002t0001g0079 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1004+2229C>T | TBX18 | ENSG00000112837.17 | transcript | ENST00000369663.10 | protein_coding | 6/7 | chr6 | 84742032 | |||||||
| chr6:84742081 | A | G | 1 | a0001c0001t0005g0136 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1004+2180T>C | TBX18 | ENSG00000112837.17 | transcript | ENST00000369663.10 | protein_coding | 6/7 | chr6 | 84742081 | |||||||
| chr6:84742424 | A | T | 3 | a0001c0001t0012g0044 a0001c0001t0012g0114 a0001c0001t0012g0154 |
4 | HG02976.hp2 HG03098.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.1004+1837T>A | TBX18 | ENSG00000112837.17 | transcript | ENST00000369663.10 | protein_coding | 6/7 | chr6 | 84742424 | |||||||
| chr6:84742467 | T | G | 1 | a0002c0002t0001g0089 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1004+1794A>C | TBX18 | ENSG00000112837.17 | transcript | ENST00000369663.10 | protein_coding | 6/7 | chr6 | 84742467 | |||||||
| chr6:84742680 | T | C | 2 | a0001c0001t0002g0042 a0001c0001t0002g0150 |
3 | HG00099.hp1 HG00140.hp1 HG01167.hp1 |
intron_variant | MODIFIER | c.1004+1581A>G | TBX18 | ENSG00000112837.17 | transcript | ENST00000369663.10 | protein_coding | 6/7 | chr6 | 84742680 | |||||||
| chr6:84742749 | T | C | 66 | a0001c0001t0002g0002 a0001c0001t0002g0008 a0001c0001t0002g0013 others(63): Show |
191 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(188): Show |
intron_variant | MODIFIER | c.1004+1512A>G | TBX18 | ENSG00000112837.17 | transcript | ENST00000369663.10 | protein_coding | 6/7 | chr6 | 84742749 | |||||||
| chr6:84742768 | A | C | 1 | a0002c0002t0001g0079 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1004+1493T>G | TBX18 | ENSG00000112837.17 | transcript | ENST00000369663.10 | protein_coding | 6/7 | chr6 | 84742768 | |||||||
| chr6:84742993 | TAACAA | T | 38 | a0002c0002t0001g0001 a0002c0002t0001g0009 a0002c0002t0001g0015 others(35): Show |
98 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(95): Show |
intron_variant | MODIFIER | c.1004+1263_1004+126 others(9): Show |
TBX18 | ENSG00000112837.17 | transcript | ENST00000369663.10 | protein_coding | 6/7 | chr6 | 84742993 | |||||||
| chr6:84743007 | A | G | 1 | a0001c0001t0004g0032 | 2 | NA18963.hp1 NA18965.hp2 |
intron_variant | MODIFIER | c.1004+1254T>C | TBX18 | ENSG00000112837.17 | transcript | ENST00000369663.10 | protein_coding | 6/7 | chr6 | 84743007 | |||||||
| chr6:84743149 | C | A | 1 | a0001c0001t0002g0150 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1004+1112G>T | TBX18 | ENSG00000112837.17 | transcript | ENST00000369663.10 | protein_coding | 6/7 | chr6 | 84743149 | |||||||
| chr6:84743263 | C | T | 1 | a0001c0001t0003g0099 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1004+998G>A | TBX18 | ENSG00000112837.17 | transcript | ENST00000369663.10 | protein_coding | 6/7 | chr6 | 84743263 | |||||||
| chr6:84743407 | G | A | 2 | a0001c0001t0004g0032 a0001c0001t0004g0033 |
4 | NA18963.hp1 NA18965.hp2 NA19076.hp2 others(1): Show |
intron_variant | MODIFIER | c.1004+854C>T | TBX18 | ENSG00000112837.17 | transcript | ENST00000369663.10 | protein_coding | 6/7 | chr6 | 84743407 | |||||||
| chr6:84743525 | G | A | 1 | a0002c0002t0001g0090 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1004+736C>T | TBX18 | ENSG00000112837.17 | transcript | ENST00000369663.10 | protein_coding | 6/7 | chr6 | 84743525 | |||||||
| chr6:84743613 | TAG | T | 3 | a0001c0001t0012g0044 a0001c0001t0012g0114 a0001c0001t0012g0154 |
4 | HG02976.hp2 HG03098.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.1004+646_1004+647d others(4): Show |
TBX18 | ENSG00000112837.17 | transcript | ENST00000369663.10 | protein_coding | 6/7 | chr6 | 84743613 | |||||||
| chr6:84743646 | C | G | 3 | a0001c0001t0012g0044 a0001c0001t0012g0114 a0001c0001t0012g0154 |
4 | HG02976.hp2 HG03098.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.1004+615G>C | TBX18 | ENSG00000112837.17 | transcript | ENST00000369663.10 | protein_coding | 6/7 | chr6 | 84743646 | |||||||
| chr6:84743700 | T | C | 3 | a0001c0001t0012g0044 a0001c0001t0012g0114 a0001c0001t0012g0154 |
4 | HG02976.hp2 HG03098.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.1004+561A>G | TBX18 | ENSG00000112837.17 | transcript | ENST00000369663.10 | protein_coding | 6/7 | chr6 | 84743700 | |||||||
| chr6:84743720 | C | T | 3 | a0001c0001t0012g0044 a0001c0001t0012g0114 a0001c0001t0012g0154 |
4 | HG02976.hp2 HG03098.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.1004+541G>A | TBX18 | ENSG00000112837.17 | transcript | ENST00000369663.10 | protein_coding | 6/7 | chr6 | 84743720 | |||||||
| chr6:84743896 | T | C | 2 | a0001c0001t0010g0010 a0001c0001t0020g0115 |
7 | HG02486.hp2 HG02572.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.1004+365A>G | TBX18 | ENSG00000112837.17 | transcript | ENST00000369663.10 | protein_coding | 6/7 | chr6 | 84743896 | |||||||
| chr6:84743905 | G | A | 1 | a0001c0001t0033g0104 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1004+356C>T | TBX18 | ENSG00000112837.17 | transcript | ENST00000369663.10 | protein_coding | 6/7 | chr6 | 84743905 | |||||||
| chr6:84743989 | G | T | 1 | a0002c0002t0038g0164 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1004+272C>A | TBX18 | ENSG00000112837.17 | transcript | ENST00000369663.10 | protein_coding | 6/7 | chr6 | 84743989 | |||||||
| chr6:84744047 | G | C | 68 | a0001c0001t0002g0002 a0001c0001t0002g0008 a0001c0001t0002g0013 others(65): Show |
193 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(190): Show |
intron_variant | MODIFIER | c.1004+214C>G | TBX18 | ENSG00000112837.17 | transcript | ENST00000369663.10 | protein_coding | 6/7 | chr6 | 84744047 | |||||||
| chr6:84744064 | C | T | 63 | a0001c0001t0002g0002 a0001c0001t0002g0008 a0001c0001t0002g0013 others(60): Show |
181 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(178): Show |
intron_variant | MODIFIER | c.1004+197G>A | TBX18 | ENSG00000112837.17 | transcript | ENST00000369663.10 | protein_coding | 6/7 | chr6 | 84744064 | |||||||
| chr6:84744185 | T | TA | 8 | a0001c0001t0006g0022 a0001c0001t0006g0131 a0001c0001t0009g0021 others(5): Show |
14 | HG01106.hp1 HG01243.hp2 HG01516.hp1 others(11): Show |
intron_variant | MODIFIER | c.1004+75dupT | TBX18 | ENSG00000112837.17 | transcript | ENST00000369663.10 | protein_coding | 6/7 | chr6 | 84744185 | |||||||
| chr6:84744436 | A | T | 3 | a0001c0001t0012g0044 a0001c0001t0012g0114 a0001c0001t0012g0154 |
4 | HG02976.hp2 HG03098.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.940-111T>A | TBX18 | ENSG00000112837.17 | transcript | ENST00000369663.10 | protein_coding | 5/7 | chr6 | 84744436 | |||||||
| chr6:84744518 | T | C | 1 | a0001c0001t0013g0127 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.940-193A>G | TBX18 | ENSG00000112837.17 | transcript | ENST00000369663.10 | protein_coding | 5/7 | chr6 | 84744518 | |||||||
| chr6:84744553 | C | G | 25 | a0001c0001t0002g0002 a0001c0001t0002g0008 a0001c0001t0002g0013 others(22): Show |
80 | HG00099.hp1 HG00140.hp1 HG00438.hp2 others(77): Show |
intron_variant | MODIFIER | c.940-228G>C | TBX18 | ENSG00000112837.17 | transcript | ENST00000369663.10 | protein_coding | 5/7 | chr6 | 84744553 | |||||||
| chr6:84744604 | A | G | 1 | a0001c0001t0009g0132 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.940-279T>C | TBX18 | ENSG00000112837.17 | transcript | ENST00000369663.10 | protein_coding | 5/7 | chr6 | 84744604 | |||||||
| chr6:84744617 | T | C | 1 | a0001c0001t0008g0098 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.940-292A>G | TBX18 | ENSG00000112837.17 | transcript | ENST00000369663.10 | protein_coding | 5/7 | chr6 | 84744617 | |||||||
| chr6:84744659 | T | C | 84 | a0001c0001t0002g0002 a0001c0001t0002g0008 a0001c0001t0002g0013 others(81): Show |
211 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(208): Show |
intron_variant | MODIFIER | c.940-334A>G | TBX18 | ENSG00000112837.17 | transcript | ENST00000369663.10 | protein_coding | 5/7 | chr6 | 84744659 | |||||||
| chr6:84744712 | T | C | 1 | a0001c0001t0002g0043 | 2 | HG00438.hp2 NA18967.hp1 |
intron_variant | MODIFIER | c.940-387A>G | TBX18 | ENSG00000112837.17 | transcript | ENST00000369663.10 | protein_coding | 5/7 | chr6 | 84744712 | |||||||
| chr6:84744818 | C | T | 2 | a0001c0001t0002g0139 a0001c0001t0002g0140 |
2 | NA18957.hp2 NA19002.hp1 |
intron_variant | MODIFIER | c.940-493G>A | TBX18 | ENSG00000112837.17 | transcript | ENST00000369663.10 | protein_coding | 5/7 | chr6 | 84744818 | |||||||
| chr6:84744857 | C | T | 1 | a0002c0002t0003g0061 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.940-532G>A | TBX18 | ENSG00000112837.17 | transcript | ENST00000369663.10 | protein_coding | 5/7 | chr6 | 84744857 | |||||||
| chr6:84744895 | T | C | 1 | a0001c0003t0004g0026 | 2 | NA18955.hp2 NA19063.hp2 |
intron_variant | MODIFIER | c.940-570A>G | TBX18 | ENSG00000112837.17 | transcript | ENST00000369663.10 | protein_coding | 5/7 | chr6 | 84744895 | |||||||
| chr6:84745126 | T | C | 8 | a0001c0001t0006g0022 a0001c0001t0006g0131 a0001c0001t0009g0021 others(5): Show |
14 | HG01106.hp1 HG01243.hp2 HG01516.hp1 others(11): Show |
intron_variant | MODIFIER | c.940-801A>G | TBX18 | ENSG00000112837.17 | transcript | ENST00000369663.10 | protein_coding | 5/7 | chr6 | 84745126 | |||||||
| chr6:84745313 | A | C | 1 | a0001c0001t0012g0044 | 2 | HG03540.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.940-988T>G | TBX18 | ENSG00000112837.17 | transcript | ENST00000369663.10 | protein_coding | 5/7 | chr6 | 84745313 | |||||||
| chr6:84745423 | A | G | 3 | a0001c0001t0012g0044 a0001c0001t0012g0114 a0001c0001t0012g0154 |
4 | HG02976.hp2 HG03098.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.940-1098T>C | TBX18 | ENSG00000112837.17 | transcript | ENST00000369663.10 | protein_coding | 5/7 | chr6 | 84745423 | |||||||
| chr6:84745550 | T | G | 1 | a0002c0002t0001g0090 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.940-1225A>C | TBX18 | ENSG00000112837.17 | transcript | ENST00000369663.10 | protein_coding | 5/7 | chr6 | 84745550 | |||||||
| chr6:84745586 | T | A | 3 | a0001c0001t0012g0044 a0001c0001t0012g0114 a0001c0001t0012g0154 |
4 | HG02976.hp2 HG03098.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.940-1261A>T | TBX18 | ENSG00000112837.17 | transcript | ENST00000369663.10 | protein_coding | 5/7 | chr6 | 84745586 | |||||||
| chr6:84745675 | C | T | 3 | a0001c0001t0012g0044 a0001c0001t0012g0114 a0001c0001t0012g0154 |
4 | HG02976.hp2 HG03098.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.940-1350G>A | TBX18 | ENSG00000112837.17 | transcript | ENST00000369663.10 | protein_coding | 5/7 | chr6 | 84745675 | |||||||
| chr6:84745846 | C | T | 5 | a0001c0001t0007g0014 a0001c0001t0007g0018 a0001c0001t0007g0160 others(2): Show |
12 | HG00741.hp2 HG02257.hp2 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.940-1521G>A | TBX18 | ENSG00000112837.17 | transcript | ENST00000369663.10 | protein_coding | 5/7 | chr6 | 84745846 | |||||||
| chr6:84745860 | C | T | 1 | a0001c0001t0005g0040 | 2 | NA18992.hp1 NA19058.hp2 |
intron_variant | MODIFIER | c.940-1535G>A | TBX18 | ENSG00000112837.17 | transcript | ENST00000369663.10 | protein_coding | 5/7 | chr6 | 84745860 | |||||||
| chr6:84745916 | T | C | 3 | a0001c0001t0012g0044 a0001c0001t0012g0114 a0001c0001t0012g0154 |
4 | HG02976.hp2 HG03098.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.940-1591A>G | TBX18 | ENSG00000112837.17 | transcript | ENST00000369663.10 | protein_coding | 5/7 | chr6 | 84745916 | |||||||
| chr6:84745988 | A | G | 1 | a0002c0002t0003g0060 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.940-1663T>C | TBX18 | ENSG00000112837.17 | transcript | ENST00000369663.10 | protein_coding | 5/7 | chr6 | 84745988 | |||||||
| chr6:84746031 | A | C | 13 | a0001c0001t0006g0022 a0001c0001t0006g0131 a0001c0001t0007g0014 others(10): Show |
26 | HG00741.hp2 HG01106.hp1 HG01243.hp2 others(23): Show |
intron_variant | MODIFIER | c.940-1706T>G | TBX18 | ENSG00000112837.17 | transcript | ENST00000369663.10 | protein_coding | 5/7 | chr6 | 84746031 | |||||||
| chr6:84746130 | G | A | 8 | a0001c0001t0006g0022 a0001c0001t0006g0131 a0001c0001t0009g0021 others(5): Show |
14 | HG01106.hp1 HG01243.hp2 HG01516.hp1 others(11): Show |
intron_variant | MODIFIER | c.939+1790C>T | TBX18 | ENSG00000112837.17 | transcript | ENST00000369663.10 | protein_coding | 5/7 | chr6 | 84746130 | |||||||
| chr6:84746132 | T | C | 3 | a0001c0001t0012g0044 a0001c0001t0012g0114 a0001c0001t0012g0154 |
4 | HG02976.hp2 HG03098.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.939+1788A>G | TBX18 | ENSG00000112837.17 | transcript | ENST00000369663.10 | protein_coding | 5/7 | chr6 | 84746132 | |||||||
| chr6:84746135 | T | C | 1 | a0002c0002t0038g0164 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.939+1785A>G | TBX18 | ENSG00000112837.17 | transcript | ENST00000369663.10 | protein_coding | 5/7 | chr6 | 84746135 | |||||||
| chr6:84746145 | T | A | 22 | a0002c0002t0001g0062 a0002c0002t0003g0004 a0002c0002t0003g0028 others(19): Show |
51 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(48): Show |
intron_variant | MODIFIER | c.939+1775A>T | TBX18 | ENSG00000112837.17 | transcript | ENST00000369663.10 | protein_coding | 5/7 | chr6 | 84746145 | |||||||
| chr6:84746186 | G | C | 1 | a0002c0002t0003g0068 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.939+1734C>G | TBX18 | ENSG00000112837.17 | transcript | ENST00000369663.10 | protein_coding | 5/7 | chr6 | 84746186 | |||||||
| chr6:84746202 | A | G | 1 | a0006c0013t0036g0126 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.939+1718T>C | TBX18 | ENSG00000112837.17 | transcript | ENST00000369663.10 | protein_coding | 5/7 | chr6 | 84746202 | |||||||
| chr6:84746214 | T | C | 37 | a0002c0002t0001g0001 a0002c0002t0001g0009 a0002c0002t0001g0015 others(34): Show |
97 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(94): Show |
intron_variant | MODIFIER | c.939+1706A>G | TBX18 | ENSG00000112837.17 | transcript | ENST00000369663.10 | protein_coding | 5/7 | chr6 | 84746214 | |||||||
| chr6:84746332 | C | T | 1 | a0009c0010t0006g0095 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.939+1588G>A | TBX18 | ENSG00000112837.17 | transcript | ENST00000369663.10 | protein_coding | 5/7 | chr6 | 84746332 | |||||||
| chr6:84746370 | C | T | 3 | a0001c0001t0012g0044 a0001c0001t0012g0114 a0001c0001t0012g0154 |
4 | HG02976.hp2 HG03098.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.939+1550G>A | TBX18 | ENSG00000112837.17 | transcript | ENST00000369663.10 | protein_coding | 5/7 | chr6 | 84746370 | |||||||
| chr6:84746434 | T | C | 4 | a0001c0001t0008g0007 a0001c0001t0008g0098 a0001c0001t0008g0105 others(1): Show |
11 | HG01891.hp1 HG01891.hp2 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.939+1486A>G | TBX18 | ENSG00000112837.17 | transcript | ENST00000369663.10 | protein_coding | 5/7 | chr6 | 84746434 | |||||||
| chr6:84746451 | C | T | 1 | a0002c0002t0001g0082 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.939+1469G>A | TBX18 | ENSG00000112837.17 | transcript | ENST00000369663.10 | protein_coding | 5/7 | chr6 | 84746451 | |||||||
| chr6:84746664 | C | A | 138 | a0001c0001t0002g0002 a0001c0001t0002g0008 a0001c0001t0002g0013 others(135): Show |
339 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(336): Show |
intron_variant | MODIFIER | c.939+1256G>T | TBX18 | ENSG00000112837.17 | transcript | ENST00000369663.10 | protein_coding | 5/7 | chr6 | 84746664 | |||||||
| chr6:84746677 | T | C | 1 | a0001c0001t0006g0131 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.939+1243A>G | TBX18 | ENSG00000112837.17 | transcript | ENST00000369663.10 | protein_coding | 5/7 | chr6 | 84746677 | |||||||
| chr6:84746795 | T | C | 1 | a0002c0002t0001g0020 | 3 | HG00735.hp1 HG01255.hp1 HG01978.hp2 |
intron_variant | MODIFIER | c.939+1125A>G | TBX18 | ENSG00000112837.17 | transcript | ENST00000369663.10 | protein_coding | 5/7 | chr6 | 84746795 | |||||||
| chr6:84746871 | A | T | 2 | a0001c0001t0002g0013 a0001c0001t0002g0147 |
6 | HG02056.hp1 NA18747.hp1 NA18975.hp1 others(3): Show |
intron_variant | MODIFIER | c.939+1049T>A | TBX18 | ENSG00000112837.17 | transcript | ENST00000369663.10 | protein_coding | 5/7 | chr6 | 84746871 | |||||||
| chr6:84747001 | C | T | 1 | a0001c0001t0012g0114 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.939+919G>A | TBX18 | ENSG00000112837.17 | transcript | ENST00000369663.10 | protein_coding | 5/7 | chr6 | 84747001 | |||||||
| chr6:84747185 | G | GA | 19 | a0001c0001t0003g0099 a0001c0001t0006g0030 a0001c0001t0006g0031 others(16): Show |
21 | HG01109.hp1 HG01884.hp1 HG02280.hp1 others(18): Show |
intron_variant | MODIFIER | c.939+734dupT | TBX18 | ENSG00000112837.17 | transcript | ENST00000369663.10 | protein_coding | 5/7 | chr6 | 84747185 | |||||||
| chr6:84747233 | A | C | 3 | a0001c0001t0012g0044 a0001c0001t0012g0114 a0001c0001t0012g0154 |
4 | HG02976.hp2 HG03098.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.939+687T>G | TBX18 | ENSG00000112837.17 | transcript | ENST00000369663.10 | protein_coding | 5/7 | chr6 | 84747233 | |||||||
| chr6:84747397 | A | C | 2 | a0001c0001t0009g0021 a0001c0001t0009g0130 |
4 | HG02723.hp1 HG02818.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.939+523T>G | TBX18 | ENSG00000112837.17 | transcript | ENST00000369663.10 | protein_coding | 5/7 | chr6 | 84747397 | |||||||
| chr6:84747469 | T | C | 2 | a0001c0001t0012g0044 a0001c0001t0012g0154 |
3 | HG02976.hp2 HG03540.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.939+451A>G | TBX18 | ENSG00000112837.17 | transcript | ENST00000369663.10 | protein_coding | 5/7 | chr6 | 84747469 | |||||||
| chr6:84747663 | T | TATC | 138 | a0001c0001t0002g0002 a0001c0001t0002g0008 a0001c0001t0002g0013 others(135): Show |
339 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(336): Show |
intron_variant | MODIFIER | c.939+256_939+257ins others(3): Show |
TBX18 | ENSG00000112837.17 | transcript | ENST00000369663.10 | protein_coding | 5/7 | chr6 | 84747663 | |||||||
| chr6:84747816 | C | A | 1 | a0001c0001t0011g0151 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.939+104G>T | TBX18 | ENSG00000112837.17 | transcript | ENST00000369663.10 | protein_coding | 5/7 | chr6 | 84747816 | |||||||
| chr6:84747817 | A | G | 1 | a0001c0001t0002g0146 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.939+103T>C | TBX18 | ENSG00000112837.17 | transcript | ENST00000369663.10 | protein_coding | 5/7 | chr6 | 84747817 | |||||||
| chr6:84747853 | G | A | 1 | a0001c0001t0006g0110 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.939+67C>T | TBX18 | ENSG00000112837.17 | transcript | ENST00000369663.10 | protein_coding | 5/7 | chr6 | 84747853 | |||||||
| chr6:84747877 | T | C | 1 | a0002c0002t0001g0029 | 2 | NA18968.hp1 NA19058.hp1 |
intron_variant | MODIFIER | c.939+43A>G | TBX18 | ENSG00000112837.17 | transcript | ENST00000369663.10 | protein_coding | 5/7 | chr6 | 84747877 | |||||||
| chr6:84747888 | A | G | 3 | a0001c0001t0012g0044 a0001c0001t0012g0114 a0001c0001t0012g0154 |
4 | HG02976.hp2 HG03098.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.939+32T>C | TBX18 | ENSG00000112837.17 | transcript | ENST00000369663.10 | protein_coding | 5/7 | chr6 | 84747888 | |||||||
| chr6:84748286 | A | G | 1 | a0001c0001t0012g0114 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.772-199T>C | TBX18 | ENSG00000112837.17 | transcript | ENST00000369663.10 | protein_coding | 4/7 | chr6 | 84748286 | |||||||
| chr6:84748335 | A | G | 4 | a0001c0001t0006g0030 a0001c0001t0012g0103 a0001c0001t0030g0102 others(1): Show |
5 | HG01884.hp1 HG02280.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.772-248T>C | TBX18 | ENSG00000112837.17 | transcript | ENST00000369663.10 | protein_coding | 4/7 | chr6 | 84748335 | |||||||
| chr6:84748340 | A | C | 2 | a0001c0001t0004g0120 a0001c0001t0004g0121 |
2 | HG02145.hp2 HG02293.hp2 |
intron_variant | MODIFIER | c.772-253T>G | TBX18 | ENSG00000112837.17 | transcript | ENST00000369663.10 | protein_coding | 4/7 | chr6 | 84748340 | |||||||
| chr6:84748470 | C | G | 1 | a0002c0002t0001g0080 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.772-383G>C | TBX18 | ENSG00000112837.17 | transcript | ENST00000369663.10 | protein_coding | 4/7 | chr6 | 84748470 | |||||||
| chr6:84748627 | G | A | 2 | a0001c0001t0009g0132 a0001c0001t0009g0133 |
2 | HG02109.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.772-540C>T | TBX18 | ENSG00000112837.17 | transcript | ENST00000369663.10 | protein_coding | 4/7 | chr6 | 84748627 | |||||||
| chr6:84748742 | C | T | 1 | a0001c0001t0003g0039 | 2 | HG03139.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.772-655G>A | TBX18 | ENSG00000112837.17 | transcript | ENST00000369663.10 | protein_coding | 4/7 | chr6 | 84748742 | |||||||
| chr6:84748745 | C | T | 1 | a0002c0002t0001g0079 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.772-658G>A | TBX18 | ENSG00000112837.17 | transcript | ENST00000369663.10 | protein_coding | 4/7 | chr6 | 84748745 | |||||||
| chr6:84748889 | A | T | 1 | a0002c0002t0001g0078 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.772-802T>A | TBX18 | ENSG00000112837.17 | transcript | ENST00000369663.10 | protein_coding | 4/7 | chr6 | 84748889 | |||||||
| chr6:84748948 | T | G | 1 | a0002c0002t0001g0092 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.772-861A>C | TBX18 | ENSG00000112837.17 | transcript | ENST00000369663.10 | protein_coding | 4/7 | chr6 | 84748948 | |||||||
| chr6:84749066 | C | T | 1 | a0002c0002t0001g0077 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.772-979G>A | TBX18 | ENSG00000112837.17 | transcript | ENST00000369663.10 | protein_coding | 4/7 | chr6 | 84749066 | |||||||
| chr6:84749280 | G | T | 1 | a0002c0002t0001g0092 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.772-1193C>A | TBX18 | ENSG00000112837.17 | transcript | ENST00000369663.10 | protein_coding | 4/7 | chr6 | 84749280 | |||||||
| chr6:84749487 | C | T | 3 | a0001c0001t0012g0044 a0001c0001t0012g0114 a0001c0001t0012g0154 |
4 | HG02976.hp2 HG03098.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.772-1400G>A | TBX18 | ENSG00000112837.17 | transcript | ENST00000369663.10 | protein_coding | 4/7 | chr6 | 84749487 | |||||||
| chr6:84749487 | CT | C | 64 | a0001c0001t0002g0002 a0001c0001t0002g0008 a0001c0001t0002g0013 others(61): Show |
182 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(179): Show |
intron_variant | MODIFIER | c.772-1401delA | TBX18 | ENSG00000112837.17 | transcript | ENST00000369663.10 | protein_coding | 4/7 | chr6 | 84749487 | |||||||
| chr6:84749550 | T | C | 1 | a0001c0001t0003g0099 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.772-1463A>G | TBX18 | ENSG00000112837.17 | transcript | ENST00000369663.10 | protein_coding | 4/7 | chr6 | 84749550 | |||||||
| chr6:84749630 | A | T | 1 | a0002c0002t0001g0076 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.772-1543T>A | TBX18 | ENSG00000112837.17 | transcript | ENST00000369663.10 | protein_coding | 4/7 | chr6 | 84749630 | |||||||
| chr6:84749709 | T | C | 138 | a0001c0001t0002g0002 a0001c0001t0002g0008 a0001c0001t0002g0013 others(135): Show |
339 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(336): Show |
intron_variant | MODIFIER | c.772-1622A>G | TBX18 | ENSG00000112837.17 | transcript | ENST00000369663.10 | protein_coding | 4/7 | chr6 | 84749709 | |||||||
| chr6:84749907 | C | G | 1 | a0002c0002t0001g0075 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.772-1820G>C | TBX18 | ENSG00000112837.17 | transcript | ENST00000369663.10 | protein_coding | 4/7 | chr6 | 84749907 | |||||||
| chr6:84750155 | C | A | 1 | a0001c0001t0012g0154 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.772-2068G>T | TBX18 | ENSG00000112837.17 | transcript | ENST00000369663.10 | protein_coding | 4/7 | chr6 | 84750155 | |||||||
| chr6:84750156 | A | G | 3 | a0001c0001t0012g0044 a0001c0001t0012g0114 a0001c0001t0012g0154 |
4 | HG02976.hp2 HG03098.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.772-2069T>C | TBX18 | ENSG00000112837.17 | transcript | ENST00000369663.10 | protein_coding | 4/7 | chr6 | 84750156 | |||||||
| chr6:84750198 | T | C | 3 | a0001c0001t0006g0030 a0001c0001t0012g0103 a0001c0001t0030g0102 |
4 | HG01884.hp1 HG02280.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.772-2111A>G | TBX18 | ENSG00000112837.17 | transcript | ENST00000369663.10 | protein_coding | 4/7 | chr6 | 84750198 | |||||||
| chr6:84750264 | A | C | 84 | a0001c0001t0002g0002 a0001c0001t0002g0008 a0001c0001t0002g0013 others(81): Show |
211 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(208): Show |
intron_variant | MODIFIER | c.772-2177T>G | TBX18 | ENSG00000112837.17 | transcript | ENST00000369663.10 | protein_coding | 4/7 | chr6 | 84750264 | |||||||
| chr6:84750266 | A | G | 1 | a0002c0002t0001g0074 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.772-2179T>C | TBX18 | ENSG00000112837.17 | transcript | ENST00000369663.10 | protein_coding | 4/7 | chr6 | 84750266 | |||||||
| chr6:84750283 | C | CA | 55 | a0001c0001t0002g0024 a0001c0001t0003g0099 a0001c0001t0004g0125 others(52): Show |
110 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(107): Show |
intron_variant | MODIFIER | c.772-2197dupT | TBX18 | ENSG00000112837.17 | transcript | ENST00000369663.10 | protein_coding | 4/7 | chr6 | 84750283 | |||||||
| chr6:84750283 | C | CAA | 15 | a0001c0001t0006g0022 a0001c0001t0006g0131 a0001c0001t0007g0014 others(12): Show |
35 | HG00741.hp2 HG01106.hp1 HG01123.hp1 others(32): Show |
intron_variant | MODIFIER | c.772-2198_772-2197d others(4): Show |
TBX18 | ENSG00000112837.17 | transcript | ENST00000369663.10 | protein_coding | 4/7 | chr6 | 84750283 | |||||||
| chr6:84750283 | CA | C | 6 | a0001c0001t0002g0145 a0001c0001t0004g0118 a0001c0001t0013g0037 others(3): Show |
8 | HG03239.hp1 HG03471.hp2 NA18955.hp2 others(5): Show |
intron_variant | MODIFIER | c.772-2197delT | TBX18 | ENSG00000112837.17 | transcript | ENST00000369663.10 | protein_coding | 4/7 | chr6 | 84750283 | |||||||
| chr6:84750362 | A | C | 1 | a0002c0002t0003g0058 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.772-2275T>G | TBX18 | ENSG00000112837.17 | transcript | ENST00000369663.10 | protein_coding | 4/7 | chr6 | 84750362 | |||||||
| chr6:84750408 | A | G | 1 | a0001c0001t0004g0120 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.772-2321T>C | TBX18 | ENSG00000112837.17 | transcript | ENST00000369663.10 | protein_coding | 4/7 | chr6 | 84750408 | |||||||
| chr6:84750777 | G | A | 3 | a0001c0001t0012g0044 a0001c0001t0012g0114 a0001c0001t0012g0154 |
4 | HG02976.hp2 HG03098.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.772-2690C>T | TBX18 | ENSG00000112837.17 | transcript | ENST00000369663.10 | protein_coding | 4/7 | chr6 | 84750777 | |||||||
| chr6:84750993 | T | C | 5 | a0001c0001t0007g0014 a0001c0001t0007g0018 a0001c0001t0007g0160 others(2): Show |
12 | HG00741.hp2 HG02257.hp2 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.772-2906A>G | TBX18 | ENSG00000112837.17 | transcript | ENST00000369663.10 | protein_coding | 4/7 | chr6 | 84750993 | |||||||
| chr6:84751349 | G | T | 1 | a0001c0001t0009g0021 | 3 | HG02723.hp1 NA18522.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.772-3262C>A | TBX18 | ENSG00000112837.17 | transcript | ENST00000369663.10 | protein_coding | 4/7 | chr6 | 84751349 | |||||||
| chr6:84751703 | T | G | 1 | a0001c0001t0005g0040 | 2 | NA18992.hp1 NA19058.hp2 |
intron_variant | MODIFIER | c.772-3616A>C | TBX18 | ENSG00000112837.17 | transcript | ENST00000369663.10 | protein_coding | 4/7 | chr6 | 84751703 | |||||||
| chr6:84752040 | T | A | 1 | a0001c0001t0022g0116 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.772-3953A>T | TBX18 | ENSG00000112837.17 | transcript | ENST00000369663.10 | protein_coding | 4/7 | chr6 | 84752040 | |||||||
| chr6:84752082 | T | C | 69 | a0001c0001t0002g0002 a0001c0001t0002g0008 a0001c0001t0002g0013 others(66): Show |
164 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(161): Show |
intron_variant | MODIFIER | c.772-3995A>G | TBX18 | ENSG00000112837.17 | transcript | ENST00000369663.10 | protein_coding | 4/7 | chr6 | 84752082 | |||||||
| chr6:84752186 | CA | C | 34 | a0001c0001t0002g0144 a0001c0001t0003g0005 a0001c0001t0003g0039 others(31): Show |
82 | HG00099.hp2 HG00639.hp2 HG00741.hp2 others(79): Show |
intron_variant | MODIFIER | c.772-4100delT | TBX18 | ENSG00000112837.17 | transcript | ENST00000369663.10 | protein_coding | 4/7 | chr6 | 84752186 | |||||||
| chr6:84752193 | A | C | 1 | a0002c0002t0003g0057 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.772-4106T>G | TBX18 | ENSG00000112837.17 | transcript | ENST00000369663.10 | protein_coding | 4/7 | chr6 | 84752193 | |||||||
| chr6:84752240 | T | A | 1 | a0002c0002t0001g0048 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.772-4153A>T | TBX18 | ENSG00000112837.17 | transcript | ENST00000369663.10 | protein_coding | 4/7 | chr6 | 84752240 | |||||||
| chr6:84752487 | A | G | 1 | a0001c0001t0002g0041 | 2 | HG01175.hp2 HG03688.hp2 |
intron_variant | MODIFIER | c.771+4211T>C | TBX18 | ENSG00000112837.17 | transcript | ENST00000369663.10 | protein_coding | 4/7 | chr6 | 84752487 | |||||||
| chr6:84752819 | G | T | 1 | a0006c0013t0036g0126 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.771+3879C>A | TBX18 | ENSG00000112837.17 | transcript | ENST00000369663.10 | protein_coding | 4/7 | chr6 | 84752819 | |||||||
| chr6:84752922 | C | T | 135 | a0001c0001t0002g0002 a0001c0001t0002g0008 a0001c0001t0002g0013 others(132): Show |
330 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(327): Show |
intron_variant | MODIFIER | c.771+3776G>A | TBX18 | ENSG00000112837.17 | transcript | ENST00000369663.10 | protein_coding | 4/7 | chr6 | 84752922 | |||||||
| chr6:84753153 | A | C | 1 | a0006c0013t0036g0126 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.771+3545T>G | TBX18 | ENSG00000112837.17 | transcript | ENST00000369663.10 | protein_coding | 4/7 | chr6 | 84753153 | |||||||
| chr6:84753315 | A | G | 1 | a0002c0002t0003g0056 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.771+3383T>C | TBX18 | ENSG00000112837.17 | transcript | ENST00000369663.10 | protein_coding | 4/7 | chr6 | 84753315 | |||||||
| chr6:84753439 | G | GA | 102 | a0001c0001t0002g0002 a0001c0001t0002g0008 a0001c0001t0002g0013 others(99): Show |
258 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(255): Show |
intron_variant | MODIFIER | c.771+3258dupT | TBX18 | ENSG00000112837.17 | transcript | ENST00000369663.10 | protein_coding | 4/7 | chr6 | 84753439 | |||||||
| chr6:84753439 | G | GAA | 34 | a0001c0001t0003g0005 a0001c0001t0003g0039 a0001c0001t0003g0134 others(31): Show |
79 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(76): Show |
intron_variant | MODIFIER | c.771+3257_771+3258d others(4): Show |
TBX18 | ENSG00000112837.17 | transcript | ENST00000369663.10 | protein_coding | 4/7 | chr6 | 84753439 | |||||||
| chr6:84753478 | A | T | 1 | a0001c0001t0012g0154 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.771+3220T>A | TBX18 | ENSG00000112837.17 | transcript | ENST00000369663.10 | protein_coding | 4/7 | chr6 | 84753478 | |||||||
| chr6:84753499 | C | G | 2 | a0001c0001t0004g0118 a0001c0001t0004g0119 |
2 | NA18941.hp1 NA18993.hp2 |
intron_variant | MODIFIER | c.771+3199G>C | TBX18 | ENSG00000112837.17 | transcript | ENST00000369663.10 | protein_coding | 4/7 | chr6 | 84753499 | |||||||
| chr6:84753589 | G | T | 1 | a0001c0001t0006g0031 | 2 | HG02922.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.771+3109C>A | TBX18 | ENSG00000112837.17 | transcript | ENST00000369663.10 | protein_coding | 4/7 | chr6 | 84753589 | |||||||
| chr6:84753799 | T | C | 25 | a0001c0001t0002g0002 a0001c0001t0002g0008 a0001c0001t0002g0013 others(22): Show |
80 | HG00099.hp1 HG00140.hp1 HG00438.hp2 others(77): Show |
intron_variant | MODIFIER | c.771+2899A>G | TBX18 | ENSG00000112837.17 | transcript | ENST00000369663.10 | protein_coding | 4/7 | chr6 | 84753799 | |||||||
| chr6:84753814 | G | C | 1 | a0002c0002t0003g0028 | 2 | HG00140.hp2 HG01074.hp2 |
intron_variant | MODIFIER | c.771+2884C>G | TBX18 | ENSG00000112837.17 | transcript | ENST00000369663.10 | protein_coding | 4/7 | chr6 | 84753814 | |||||||
| chr6:84753949 | G | A | 21 | a0001c0001t0003g0005 a0001c0001t0003g0039 a0001c0001t0003g0134 others(18): Show |
55 | HG00099.hp2 HG00639.hp2 HG01070.hp2 others(52): Show |
intron_variant | MODIFIER | c.771+2749C>T | TBX18 | ENSG00000112837.17 | transcript | ENST00000369663.10 | protein_coding | 4/7 | chr6 | 84753949 | |||||||
| chr6:84753996 | C | G | 25 | a0001c0001t0002g0002 a0001c0001t0002g0008 a0001c0001t0002g0013 others(22): Show |
80 | HG00099.hp1 HG00140.hp1 HG00438.hp2 others(77): Show |
intron_variant | MODIFIER | c.771+2702G>C | TBX18 | ENSG00000112837.17 | transcript | ENST00000369663.10 | protein_coding | 4/7 | chr6 | 84753996 | |||||||
| chr6:84754010 | C | T | 1 | a0001c0001t0029g0106 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.771+2688G>A | TBX18 | ENSG00000112837.17 | transcript | ENST00000369663.10 | protein_coding | 4/7 | chr6 | 84754010 | |||||||
| chr6:84754223 | C | G | 1 | a0001c0001t0002g0143 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.771+2475G>C | TBX18 | ENSG00000112837.17 | transcript | ENST00000369663.10 | protein_coding | 4/7 | chr6 | 84754223 | |||||||
| chr6:84754426 | C | T | 1 | a0002c0002t0023g0053 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.771+2272G>A | TBX18 | ENSG00000112837.17 | transcript | ENST00000369663.10 | protein_coding | 4/7 | chr6 | 84754426 | |||||||
| chr6:84754544 | G | A | 7 | a0001c0001t0004g0012 a0001c0001t0005g0006 a0001c0001t0005g0011 others(4): Show |
25 | HG00099.hp2 HG00639.hp2 HG01070.hp2 others(22): Show |
intron_variant | MODIFIER | c.771+2154C>T | TBX18 | ENSG00000112837.17 | transcript | ENST00000369663.10 | protein_coding | 4/7 | chr6 | 84754544 | |||||||
| chr6:84754574 | T | C | 1 | a0001c0001t0002g0152 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.771+2124A>G | TBX18 | ENSG00000112837.17 | transcript | ENST00000369663.10 | protein_coding | 4/7 | chr6 | 84754574 | |||||||
| chr6:84754663 | T | C | 1 | a0006c0013t0036g0126 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.771+2035A>G | TBX18 | ENSG00000112837.17 | transcript | ENST00000369663.10 | protein_coding | 4/7 | chr6 | 84754663 | |||||||
| chr6:84754738 | A | G | 1 | a0006c0013t0036g0126 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.771+1960T>C | TBX18 | ENSG00000112837.17 | transcript | ENST00000369663.10 | protein_coding | 4/7 | chr6 | 84754738 | |||||||
| chr6:84754777 | G | A | 1 | a0001c0001t0007g0018 | 4 | HG02895.hp1 HG02897.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.771+1921C>T | TBX18 | ENSG00000112837.17 | transcript | ENST00000369663.10 | protein_coding | 4/7 | chr6 | 84754777 | |||||||
| chr6:84754916 | A | G | 13 | a0001c0001t0003g0005 a0001c0001t0003g0039 a0001c0001t0003g0134 others(10): Show |
29 | HG01106.hp1 HG01168.hp2 HG01243.hp2 others(26): Show |
intron_variant | MODIFIER | c.771+1782T>C | TBX18 | ENSG00000112837.17 | transcript | ENST00000369663.10 | protein_coding | 4/7 | chr6 | 84754916 | |||||||
| chr6:84754947 | T | C | 1 | a0004c0006t0006g0101 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.771+1751A>G | TBX18 | ENSG00000112837.17 | transcript | ENST00000369663.10 | protein_coding | 4/7 | chr6 | 84754947 | |||||||
| chr6:84755060 | C | T | 1 | a0001c0001t0016g0109 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.771+1638G>A | TBX18 | ENSG00000112837.17 | transcript | ENST00000369663.10 | protein_coding | 4/7 | chr6 | 84755060 | |||||||
| chr6:84755092 | TTAAA | T | 7 | a0001c0001t0004g0012 a0001c0001t0005g0006 a0001c0001t0005g0011 others(4): Show |
25 | HG00099.hp2 HG00639.hp2 HG01070.hp2 others(22): Show |
intron_variant | MODIFIER | c.771+1602_771+1605d others(6): Show |
TBX18 | ENSG00000112837.17 | transcript | ENST00000369663.10 | protein_coding | 4/7 | chr6 | 84755092 | |||||||
| chr6:84755123 | A | T | 1 | a0001c0001t0004g0117 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.771+1575T>A | TBX18 | ENSG00000112837.17 | transcript | ENST00000369663.10 | protein_coding | 4/7 | chr6 | 84755123 | |||||||
| chr6:84755124 | T | TATC | 139 | a0001c0001t0002g0002 a0001c0001t0002g0008 a0001c0001t0002g0013 others(136): Show |
340 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(337): Show |
intron_variant | MODIFIER | c.771+1573_771+1574i others(5): Show |
TBX18 | ENSG00000112837.17 | transcript | ENST00000369663.10 | protein_coding | 4/7 | chr6 | 84755124 | |||||||
| chr6:84755188 | A | G | 1 | a0001c0001t0002g0142 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.771+1510T>C | TBX18 | ENSG00000112837.17 | transcript | ENST00000369663.10 | protein_coding | 4/7 | chr6 | 84755188 | |||||||
| chr6:84755463 | C | T | 5 | a0001c0001t0003g0005 a0001c0001t0003g0039 a0001c0001t0003g0134 others(2): Show |
15 | HG01168.hp2 HG02258.hp2 HG02300.hp1 others(12): Show |
intron_variant | MODIFIER | c.771+1235G>A | TBX18 | ENSG00000112837.17 | transcript | ENST00000369663.10 | protein_coding | 4/7 | chr6 | 84755463 | |||||||
| chr6:84755810 | A | G | 21 | a0001c0001t0003g0099 a0001c0001t0006g0030 a0001c0001t0006g0031 others(18): Show |
30 | HG01109.hp1 HG01884.hp1 HG01891.hp1 others(27): Show |
intron_variant | MODIFIER | c.771+888T>C | TBX18 | ENSG00000112837.17 | transcript | ENST00000369663.10 | protein_coding | 4/7 | chr6 | 84755810 | |||||||
| chr6:84755813 | C | A | 7 | a0001c0001t0004g0012 a0001c0001t0005g0006 a0001c0001t0005g0011 others(4): Show |
25 | HG00099.hp2 HG00639.hp2 HG01070.hp2 others(22): Show |
intron_variant | MODIFIER | c.771+885G>T | TBX18 | ENSG00000112837.17 | transcript | ENST00000369663.10 | protein_coding | 4/7 | chr6 | 84755813 | |||||||
| chr6:84755840 | G | T | 2 | a0001c0001t0006g0030 a0001c0001t0012g0103 |
3 | HG01884.hp1 HG02280.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.771+858C>A | TBX18 | ENSG00000112837.17 | transcript | ENST00000369663.10 | protein_coding | 4/7 | chr6 | 84755840 | |||||||
| chr6:84756000 | A | C | 1 | a0001c0001t0002g0141 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.771+698T>G | TBX18 | ENSG00000112837.17 | transcript | ENST00000369663.10 | protein_coding | 4/7 | chr6 | 84756000 | |||||||
| chr6:84756006 | C | T | 1 | a0001c0001t0022g0116 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.771+692G>A | TBX18 | ENSG00000112837.17 | transcript | ENST00000369663.10 | protein_coding | 4/7 | chr6 | 84756006 | |||||||
| chr6:84756262 | T | C | 59 | a0002c0002t0001g0001 a0002c0002t0001g0009 a0002c0002t0001g0015 others(56): Show |
148 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(145): Show |
intron_variant | MODIFIER | c.771+436A>G | TBX18 | ENSG00000112837.17 | transcript | ENST00000369663.10 | protein_coding | 4/7 | chr6 | 84756262 | |||||||
| chr6:84756399 | A | G | 1 | a0001c0001t0022g0116 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.771+299T>C | TBX18 | ENSG00000112837.17 | transcript | ENST00000369663.10 | protein_coding | 4/7 | chr6 | 84756399 | |||||||
| chr6:84756469 | T | A | 21 | a0001c0001t0003g0099 a0001c0001t0006g0030 a0001c0001t0006g0031 others(18): Show |
30 | HG01109.hp1 HG01884.hp1 HG01891.hp1 others(27): Show |
intron_variant | MODIFIER | c.771+229A>T | TBX18 | ENSG00000112837.17 | transcript | ENST00000369663.10 | protein_coding | 4/7 | chr6 | 84756469 | |||||||
| chr6:84756568 | A | C | 101 | a0001c0001t0003g0005 a0001c0001t0003g0039 a0001c0001t0003g0099 others(98): Show |
233 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(230): Show |
intron_variant | MODIFIER | c.771+130T>G | TBX18 | ENSG00000112837.17 | transcript | ENST00000369663.10 | protein_coding | 4/7 | chr6 | 84756568 | |||||||
| chr6:84756987 | C | T | 21 | a0001c0001t0003g0099 a0001c0001t0006g0030 a0001c0001t0006g0031 others(18): Show |
30 | HG01109.hp1 HG01884.hp1 HG01891.hp1 others(27): Show |
intron_variant | MODIFIER | c.600-118G>A | TBX18 | ENSG00000112837.17 | transcript | ENST00000369663.10 | protein_coding | 3/7 | chr6 | 84756987 | |||||||
| chr6:84757072 | T | C | 1 | a0001c0001t0002g0140 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.600-203A>G | TBX18 | ENSG00000112837.17 | transcript | ENST00000369663.10 | protein_coding | 3/7 | chr6 | 84757072 | |||||||
| chr6:84757078 | C | T | 1 | a0001c0014t0006g0111 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.600-209G>A | TBX18 | ENSG00000112837.17 | transcript | ENST00000369663.10 | protein_coding | 3/7 | chr6 | 84757078 | |||||||
| chr6:84757239 | C | G | 1 | a0001c0001t0008g0105 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.600-370G>C | TBX18 | ENSG00000112837.17 | transcript | ENST00000369663.10 | protein_coding | 3/7 | chr6 | 84757239 | |||||||
| chr6:84757773 | T | C | 59 | a0002c0002t0001g0001 a0002c0002t0001g0009 a0002c0002t0001g0015 others(56): Show |
148 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(145): Show |
intron_variant | MODIFIER | c.600-904A>G | TBX18 | ENSG00000112837.17 | transcript | ENST00000369663.10 | protein_coding | 3/7 | chr6 | 84757773 | |||||||
| chr6:84757850 | TTAGA | T | 1 | a0001c0001t0002g0008 | 8 | NA18949.hp2 NA18952.hp2 NA18972.hp2 others(5): Show |
intron_variant | MODIFIER | c.600-985_600-982del others(4): Show |
TBX18 | ENSG00000112837.17 | transcript | ENST00000369663.10 | protein_coding | 3/7 | chr6 | 84757850 | |||||||
| chr6:84757881 | A | G | 5 | a0001c0001t0007g0014 a0001c0001t0007g0018 a0001c0001t0007g0160 others(2): Show |
12 | HG00741.hp2 HG02257.hp2 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.600-1012T>C | TBX18 | ENSG00000112837.17 | transcript | ENST00000369663.10 | protein_coding | 3/7 | chr6 | 84757881 | |||||||
| chr6:84758339 | C | T | 2 | a0001c0001t0010g0010 a0001c0001t0020g0115 |
7 | HG02486.hp2 HG02572.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.600-1470G>A | TBX18 | ENSG00000112837.17 | transcript | ENST00000369663.10 | protein_coding | 3/7 | chr6 | 84758339 | |||||||
| chr6:84758419 | A | G | 4 | a0001c0001t0006g0030 a0001c0001t0012g0103 a0001c0001t0030g0102 others(1): Show |
5 | HG01884.hp1 HG02280.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.600-1550T>C | TBX18 | ENSG00000112837.17 | transcript | ENST00000369663.10 | protein_coding | 3/7 | chr6 | 84758419 | |||||||
| chr6:84758555 | C | A | 1 | a0001c0001t0016g0109 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.600-1686G>T | TBX18 | ENSG00000112837.17 | transcript | ENST00000369663.10 | protein_coding | 3/7 | chr6 | 84758555 | |||||||
| chr6:84758635 | T | G | 25 | a0001c0001t0002g0002 a0001c0001t0002g0008 a0001c0001t0002g0013 others(22): Show |
80 | HG00099.hp1 HG00140.hp1 HG00438.hp2 others(77): Show |
intron_variant | MODIFIER | c.599+1620A>C | TBX18 | ENSG00000112837.17 | transcript | ENST00000369663.10 | protein_coding | 3/7 | chr6 | 84758635 | |||||||
| chr6:84758638 | A | C | 21 | a0001c0001t0003g0099 a0001c0001t0006g0030 a0001c0001t0006g0031 others(18): Show |
30 | HG01109.hp1 HG01884.hp1 HG01891.hp1 others(27): Show |
intron_variant | MODIFIER | c.599+1617T>G | TBX18 | ENSG00000112837.17 | transcript | ENST00000369663.10 | protein_coding | 3/7 | chr6 | 84758638 | |||||||
| chr6:84758749 | C | T | 36 | a0002c0002t0001g0001 a0002c0002t0001g0009 a0002c0002t0001g0015 others(33): Show |
96 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(93): Show |
intron_variant | MODIFIER | c.599+1506G>A | TBX18 | ENSG00000112837.17 | transcript | ENST00000369663.10 | protein_coding | 3/7 | chr6 | 84758749 | |||||||
| chr6:84758982 | T | C | 1 | a0001c0001t0002g0153 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.599+1273A>G | TBX18 | ENSG00000112837.17 | transcript | ENST00000369663.10 | protein_coding | 3/7 | chr6 | 84758982 | |||||||
| chr6:84759048 | T | G | 1 | a0001c0001t0025g0128 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.599+1207A>C | TBX18 | ENSG00000112837.17 | transcript | ENST00000369663.10 | protein_coding | 3/7 | chr6 | 84759048 | |||||||
| chr6:84759084 | T | C | 1 | a0001c0001t0007g0018 | 4 | HG02895.hp1 HG02897.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.599+1171A>G | TBX18 | ENSG00000112837.17 | transcript | ENST00000369663.10 | protein_coding | 3/7 | chr6 | 84759084 | |||||||
| chr6:84759195 | T | A | 6 | a0001c0001t0004g0012 a0001c0001t0005g0006 a0001c0001t0005g0040 others(3): Show |
19 | HG00099.hp2 HG00639.hp2 HG01070.hp2 others(16): Show |
intron_variant | MODIFIER | c.599+1060A>T | TBX18 | ENSG00000112837.17 | transcript | ENST00000369663.10 | protein_coding | 3/7 | chr6 | 84759195 | |||||||
| chr6:84759241 | C | T | 163 | a0001c0001t0001g0035 a0001c0001t0002g0002 a0001c0001t0002g0008 others(160): Show |
401 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(398): Show |
intron_variant | MODIFIER | c.599+1014G>A | TBX18 | ENSG00000112837.17 | transcript | ENST00000369663.10 | protein_coding | 3/7 | chr6 | 84759241 | |||||||
| chr6:84759301 | C | T | 2 | a0001c0001t0006g0110 a0001c0001t0009g0129 |
2 | HG01884.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.599+954G>A | TBX18 | ENSG00000112837.17 | transcript | ENST00000369663.10 | protein_coding | 3/7 | chr6 | 84759301 | |||||||
| chr6:84759363 | A | C | 1 | a0001c0001t0006g0031 | 2 | HG02922.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.599+892T>G | TBX18 | ENSG00000112837.17 | transcript | ENST00000369663.10 | protein_coding | 3/7 | chr6 | 84759363 | |||||||
| chr6:84759395 | C | G | 2 | a0002c0002t0001g0072 a0002c0002t0001g0073 |
2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.599+860G>C | TBX18 | ENSG00000112837.17 | transcript | ENST00000369663.10 | protein_coding | 3/7 | chr6 | 84759395 | |||||||
| chr6:84759469 | C | G | 1 | a0001c0001t0002g0016 | 4 | HG02074.hp2 NA18747.hp2 NA18965.hp1 others(1): Show |
intron_variant | MODIFIER | c.599+786G>C | TBX18 | ENSG00000112837.17 | transcript | ENST00000369663.10 | protein_coding | 3/7 | chr6 | 84759469 | |||||||
| chr6:84759549 | C | CA | 26 | a0001c0001t0002g0002 a0001c0001t0002g0008 a0001c0001t0002g0013 others(23): Show |
81 | HG00099.hp1 HG00140.hp1 HG00438.hp2 others(78): Show |
intron_variant | MODIFIER | c.599+705dupT | TBX18 | ENSG00000112837.17 | transcript | ENST00000369663.10 | protein_coding | 3/7 | chr6 | 84759549 | |||||||
| chr6:84759563 | G | C | 13 | a0001c0001t0003g0005 a0001c0001t0003g0039 a0001c0001t0003g0134 others(10): Show |
29 | HG01106.hp1 HG01168.hp2 HG01243.hp2 others(26): Show |
intron_variant | MODIFIER | c.599+692C>G | TBX18 | ENSG00000112837.17 | transcript | ENST00000369663.10 | protein_coding | 3/7 | chr6 | 84759563 | |||||||
| chr6:84759589 | C | T | 1 | a0001c0001t0030g0102 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.599+666G>A | TBX18 | ENSG00000112837.17 | transcript | ENST00000369663.10 | protein_coding | 3/7 | chr6 | 84759589 | |||||||
| chr6:84759690 | C | A | 7 | a0001c0001t0004g0012 a0001c0001t0005g0006 a0001c0001t0005g0011 others(4): Show |
25 | HG00099.hp2 HG00639.hp2 HG01070.hp2 others(22): Show |
intron_variant | MODIFIER | c.599+565G>T | TBX18 | ENSG00000112837.17 | transcript | ENST00000369663.10 | protein_coding | 3/7 | chr6 | 84759690 | |||||||
| chr6:84760063 | A | G | 2 | a0004c0006t0006g0100 a0004c0006t0006g0101 |
2 | HG03209.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.599+192T>C | TBX18 | ENSG00000112837.17 | transcript | ENST00000369663.10 | protein_coding | 3/7 | chr6 | 84760063 | |||||||
| chr6:84760083 | C | T | 8 | a0001c0001t0006g0022 a0001c0001t0006g0131 a0001c0001t0009g0021 others(5): Show |
14 | HG01106.hp1 HG01243.hp2 HG01516.hp1 others(11): Show |
intron_variant | MODIFIER | c.599+172G>A | TBX18 | ENSG00000112837.17 | transcript | ENST00000369663.10 | protein_coding | 3/7 | chr6 | 84760083 | |||||||
| chr6:84760093 | G | T | 1 | a0002c0002t0005g0071 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.599+162C>A | TBX18 | ENSG00000112837.17 | transcript | ENST00000369663.10 | protein_coding | 3/7 | chr6 | 84760093 | |||||||
| chr6:84760382 | G | C | 13 | a0001c0001t0003g0005 a0001c0001t0003g0039 a0001c0001t0003g0134 others(10): Show |
29 | HG01106.hp1 HG01168.hp2 HG01243.hp2 others(26): Show |
intron_variant | MODIFIER | c.498-26C>G | TBX18 | ENSG00000112837.17 | transcript | ENST00000369663.10 | protein_coding | 2/7 | chr6 | 84760382 | |||||||
| chr6:84760406 | T | A | 13 | a0001c0001t0003g0005 a0001c0001t0003g0039 a0001c0001t0003g0134 others(10): Show |
29 | HG01106.hp1 HG01168.hp2 HG01243.hp2 others(26): Show |
intron_variant | MODIFIER | c.498-50A>T | TBX18 | ENSG00000112837.17 | transcript | ENST00000369663.10 | protein_coding | 2/7 | chr6 | 84760406 | |||||||
| chr6:84760434 | A | T | 2 | a0001c0001t0002g0139 a0001c0001t0002g0140 |
2 | NA18957.hp2 NA19002.hp1 |
intron_variant | MODIFIER | c.498-78T>A | TBX18 | ENSG00000112837.17 | transcript | ENST00000369663.10 | protein_coding | 2/7 | chr6 | 84760434 | |||||||
| chr6:84760459 | T | A | 7 | a0001c0001t0004g0012 a0001c0001t0005g0006 a0001c0001t0005g0011 others(4): Show |
25 | HG00099.hp2 HG00639.hp2 HG01070.hp2 others(22): Show |
intron_variant | MODIFIER | c.498-103A>T | TBX18 | ENSG00000112837.17 | transcript | ENST00000369663.10 | protein_coding | 2/7 | chr6 | 84760459 | |||||||
| chr6:84761091 | C | T | 1 | a0001c0001t0007g0160 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.498-735G>A | TBX18 | ENSG00000112837.17 | transcript | ENST00000369663.10 | protein_coding | 2/7 | chr6 | 84761091 | |||||||
| chr6:84761211 | T | C | 1 | a0001c0001t0006g0110 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.498-855A>G | TBX18 | ENSG00000112837.17 | transcript | ENST00000369663.10 | protein_coding | 2/7 | chr6 | 84761211 | |||||||
| chr6:84761336 | A | G | 1 | a0001c0001t0003g0099 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.498-980T>C | TBX18 | ENSG00000112837.17 | transcript | ENST00000369663.10 | protein_coding | 2/7 | chr6 | 84761336 | |||||||
| chr6:84761351 | T | G | 1 | a0001c0001t0004g0135 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.498-995A>C | TBX18 | ENSG00000112837.17 | transcript | ENST00000369663.10 | protein_coding | 2/7 | chr6 | 84761351 | |||||||
| chr6:84761417 | A | G | 1 | a0002c0002t0003g0052 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.498-1061T>C | TBX18 | ENSG00000112837.17 | transcript | ENST00000369663.10 | protein_coding | 2/7 | chr6 | 84761417 | |||||||
| chr6:84761465 | T | G | 1 | a0002c0002t0003g0070 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.497+1079A>C | TBX18 | ENSG00000112837.17 | transcript | ENST00000369663.10 | protein_coding | 2/7 | chr6 | 84761465 | |||||||
| chr6:84761508 | T | G | 4 | a0001c0001t0006g0031 a0001c0001t0006g0112 a0001c0001t0008g0113 others(1): Show |
5 | HG02486.hp1 HG02723.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.497+1036A>C | TBX18 | ENSG00000112837.17 | transcript | ENST00000369663.10 | protein_coding | 2/7 | chr6 | 84761508 | |||||||
| chr6:84761546 | T | C | 22 | a0002c0002t0001g0062 a0002c0002t0003g0004 a0002c0002t0003g0028 others(19): Show |
51 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(48): Show |
intron_variant | MODIFIER | c.497+998A>G | TBX18 | ENSG00000112837.17 | transcript | ENST00000369663.10 | protein_coding | 2/7 | chr6 | 84761546 | |||||||
| chr6:84761746 | G | A | 7 | a0001c0001t0004g0012 a0001c0001t0005g0006 a0001c0001t0005g0011 others(4): Show |
25 | HG00099.hp2 HG00639.hp2 HG01070.hp2 others(22): Show |
intron_variant | MODIFIER | c.497+798C>T | TBX18 | ENSG00000112837.17 | transcript | ENST00000369663.10 | protein_coding | 2/7 | chr6 | 84761746 | |||||||
| chr6:84761822 | T | C | 5 | a0001c0001t0007g0014 a0001c0001t0007g0018 a0001c0001t0007g0160 others(2): Show |
12 | HG00741.hp2 HG02257.hp2 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.497+722A>G | TBX18 | ENSG00000112837.17 | transcript | ENST00000369663.10 | protein_coding | 2/7 | chr6 | 84761822 | |||||||
| chr6:84761862 | T | C | 1 | a0001c0001t0007g0162 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.497+682A>G | TBX18 | ENSG00000112837.17 | transcript | ENST00000369663.10 | protein_coding | 2/7 | chr6 | 84761862 | |||||||
| chr6:84762162 | G | GA | 49 | a0001c0001t0002g0002 a0001c0001t0002g0008 a0001c0001t0002g0013 others(46): Show |
133 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(130): Show |
intron_variant | MODIFIER | c.497+381dupT | TBX18 | ENSG00000112837.17 | transcript | ENST00000369663.10 | protein_coding | 2/7 | chr6 | 84762162 | |||||||
| chr6:84762291 | G | A | 3 | a0001c0001t0012g0044 a0001c0001t0012g0114 a0001c0001t0012g0154 |
4 | HG02976.hp2 HG03098.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.497+253C>T | TBX18 | ENSG00000112837.17 | transcript | ENST00000369663.10 | protein_coding | 2/7 | chr6 | 84762291 | |||||||
| chr6:84762404 | T | A | 1 | a0001c0001t0011g0155 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.497+140A>T | TBX18 | ENSG00000112837.17 | transcript | ENST00000369663.10 | protein_coding | 2/7 | chr6 | 84762404 | |||||||
| chr6:84762411 | C | T | 22 | a0002c0002t0001g0062 a0002c0002t0003g0004 a0002c0002t0003g0028 others(19): Show |
51 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(48): Show |
intron_variant | MODIFIER | c.497+133G>A | TBX18 | ENSG00000112837.17 | transcript | ENST00000369663.10 | protein_coding | 2/7 | chr6 | 84762411 | |||||||
| chr6:84762480 | G | A | 2 | a0001c0001t0003g0005 a0007c0012t0003g0156 |
11 | HG01168.hp2 HG02300.hp1 HG02698.hp2 others(8): Show |
intron_variant | MODIFIER | c.497+64C>T | TBX18 | ENSG00000112837.17 | transcript | ENST00000369663.10 | protein_coding | 2/7 | chr6 | 84762480 | |||||||
| chr6:84762823 | C | T | 1 | a0001c0001t0008g0098 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.293-75G>A | TBX18 | ENSG00000112837.17 | transcript | ENST00000369663.10 | protein_coding | 1/7 | chr6 | 84762823 | |||||||
| chr6:84762972 | C | G | 1 | a0002c0002t0001g0051 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.293-224G>C | TBX18 | ENSG00000112837.17 | transcript | ENST00000369663.10 | protein_coding | 1/7 | chr6 | 84762972 | |||||||
| chr6:84763016 | C | CCCGCTGG others(4): Show |
2 | a0001c0001t0004g0032 a0001c0001t0004g0033 |
4 | NA18963.hp1 NA18965.hp2 NA19076.hp2 others(1): Show |
intron_variant | MODIFIER | c.293-279_293-269dup others(11): Show |
TBX18 | ENSG00000112837.17 | transcript | ENST00000369663.10 | protein_coding | 1/7 | chr6 | 84763016 | |||||||
| chr6:84763179 | C | T | 21 | a0001c0001t0003g0099 a0001c0001t0006g0030 a0001c0001t0006g0031 others(18): Show |
30 | HG01109.hp1 HG01884.hp1 HG01891.hp1 others(27): Show |
intron_variant | MODIFIER | c.293-431G>A | TBX18 | ENSG00000112837.17 | transcript | ENST00000369663.10 | protein_coding | 1/7 | chr6 | 84763179 | |||||||
| chr6:84763191 | C | G | 1 | a0001c0001t0012g0114 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.293-443G>C | TBX18 | ENSG00000112837.17 | transcript | ENST00000369663.10 | protein_coding | 1/7 | chr6 | 84763191 | |||||||
| chr6:84763258 | C | G | 1 | a0002c0002t0003g0050 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.293-510G>C | TBX18 | ENSG00000112837.17 | transcript | ENST00000369663.10 | protein_coding | 1/7 | chr6 | 84763258 | |||||||
| chr6:84763522 | C | T | 1 | a0002c0002t0001g0027 | 2 | HG03704.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.292+368G>A | TBX18 | ENSG00000112837.17 | transcript | ENST00000369663.10 | protein_coding | 1/7 | chr6 | 84763522 | |||||||
| chr6:84763698 | C | G | 21 | a0001c0001t0003g0099 a0001c0001t0006g0030 a0001c0001t0006g0031 others(18): Show |
30 | HG01109.hp1 HG01884.hp1 HG01891.hp1 others(27): Show |
intron_variant | MODIFIER | c.292+192G>C | TBX18 | ENSG00000112837.17 | transcript | ENST00000369663.10 | protein_coding | 1/7 | chr6 | 84763698 | |||||||
| chr6:84763734 | A | G | 21 | a0001c0001t0003g0099 a0001c0001t0006g0030 a0001c0001t0006g0031 others(18): Show |
30 | HG01109.hp1 HG01884.hp1 HG01891.hp1 others(27): Show |
intron_variant | MODIFIER | c.292+156T>C | TBX18 | ENSG00000112837.17 | transcript | ENST00000369663.10 | protein_coding | 1/7 | chr6 | 84763734 | |||||||
| chr6:84763794 | GCCATGTA others(25): Show |
G | 1 | a0002c0002t0003g0049 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.292+64_292+95delTG others(30): Show |
TBX18 | ENSG00000112837.17 | transcript | ENST00000369663.10 | protein_coding | 1/7 | chr6 | 84763794 | |||||||
| chr6:84763804 | G | A | 1 | a0001c0001t0004g0003 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.292+86C>T | TBX18 | ENSG00000112837.17 | transcript | ENST00000369663.10 | protein_coding | 1/7 | chr6 | 84763804 | |||||||
| chr6:84763855 | G | C | 5 | a0001c0001t0007g0014 a0001c0001t0007g0018 a0001c0001t0007g0160 others(2): Show |
12 | HG00741.hp2 HG02257.hp2 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.292+35C>G | TBX18 | ENSG00000112837.17 | transcript | ENST00000369663.10 | protein_coding | 1/7 | chr6 | 84763855 | |||||||
| chr6:84763860 | G | A | 1 | a0001c0001t0002g0163 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.292+30C>T | TBX18 | ENSG00000112837.17 | transcript | ENST00000369663.10 | protein_coding | 1/7 | chr6 | 84763860 | |||||||
| chr6:84763861 | A | G | 1 | a0002c0002t0001g0048 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.292+29T>C | TBX18 | ENSG00000112837.17 | transcript | ENST00000369663.10 | protein_coding | 1/7 | chr6 | 84763861 |